ACtalent

Job Description Job Description Job Title: Purification Scientist Job Description The Purification Scientist supports a DNA/RNA purification manufacturing team focused on plasmid and vector processing. In this role, you execute established workflows to produce purified DNA while following strict standard operating procedures (SOPs) and maintaining accurate, real-time documentation. You work in a highly process-driven, fast-paced environment and contribute directly to manufacturing operations and production workflows. Responsibilities Perform agar plating, colony selection, and culture growth to support plasmid and vector production. Execute plasmid and vector purification workflows according to established protocols. Conduct DNA dilutions and prepare buffers, reagents, and other solutions required for purification processes. Handle DNA and RNA materials safely and accurately throughout the manufacturing process. Follow standard operating procedures (SOPs) consistently and precisely for all laboratory and manufacturing activities. Maintain accurate, real-time documentation of all work performed, including batch records and related manufacturing documentation. Support general manufacturing operations and production workflows as needed to meet output and quality targets. Collaborate closely with team members to ensure smooth handoffs, efficient workflow, and adherence to production schedules. Apply strong attention to detail to ensure high-quality, repeatable results in a structured manufacturing environment. Participate in training and continuous improvement activities to enhance processes and maintain best practices. Essential Skills Hands-on experience with core molecular biology techniques, including DNA/RNA handling, plasmids, and PCR. Direct experience working with DNA in a lab environment, such as purification, plasmid workflows, vector workflows, or similar processes. Demonstrated ability to follow strict standard operating procedures (SOPs) in a manufacturing or laboratory setting. Strong documentation skills with a good documentation practice (GDP) mindset and comfort documenting work in real time. Experience with plasmid purification and vector purification workflows. Familiarity with cell culture techniques in support of plasmid or vector production. Understanding of GMP or GMP-like manufacturing environments and batch record practices. Bachelor's degree in Biology, Molecular Biology, Biochemistry, or a related scientific field. Strong organizational skills and attention to detail in a process-driven environment. Ability to work comfortably with hands-on lab work and routine, repeatable processes. Effective communication and teamwork skills in a collaborative environment. Additional Skills & Qualifications Interest in building a career in biotech GMP manufacturing and DNA/RNA purification. Comfort working in a structured, highly repeatable manufacturing environment. Ability to learn new workflows quickly through a structured training plan. Strong time management skills to operate effectively in a fast-paced, production-based setting. Motivation to contribute to a collaborative, tight-knit team environment. High level of personal accountability and ownership for quality and compliance. Job Type & Location This is a Contract position based out of Carlsbad, CA. Pay and Benefits The pay range for this position is $25.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Carlsbad,CA. Application Deadline This position is anticipated to close on Jun 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: QA Analyst (2nd Shift) Job Description As a QA Analyst, you will play a crucial role in ensuring quality and compliance through auditing, evaluating materials, and driving continuous improvement efforts. Your contribution will directly impact the success of our customers by maintaining high-quality standards in our facility and production lines. Responsibilities Perform reviews of Production Batch Records to maintain a world-class manufacturing control program. Ensure documentation records are accurate and compliant with GDP requirements. Ensure compliance with current SOPs, Work Instructions, and test procedures. Train personnel to improve compliance with regulatory and quality requirements. Provide technical, process direction, and training to manufacturing personnel. Utilize interpersonal skills to foster a culture of quality and increase quality awareness. Document and investigate deviations and out-of-specification (OOS) situations. Proactively update SOPs, Work Instructions, controlled forms, and test methods to support improvements and compliance. Ensure product quality specifications and customer standards are met and maintained. Complete approvals to run as needed and document quality events for effective decision-making. Ensure products meet specifications prior to release and maintain current reference and product standards. Utilize data to focus improvement efforts and resolve ongoing quality issues on the floor. Document OOS situations, determine root causes, and suggest solutions to prevent recurrence. Maintain compliance with current regulatory expectations and practices. Implement and maintain standards and processes to eliminate waste throughout the department. Apply and utilize lean tools to permanently implement improvements. Institutionalize 5-S in all aspects of the department. Essential Skills Experience in a GMP manufacturing environment such as pharmaceuticals, medical devices, cosmetics, or food manufacturing. Experience reviewing batch records and/or compounding records. Bachelor's degree in Chemistry, Biology, or related field. GMP, batch record, Quality Assurance within the specified industries. Additional Skills & Qualifications Working knowledge of drug manufacturing regulations such as cGMP & 21CFR regulations. Experience with investigations and deviations. Strong attention to detail. Ability to multi-task. Strong sense of urgency. Strong organizational skills. Highly self-motivated with the ability to work independently. Confident communicator comfortable with making outbound calls and enforcing policies. Work Environment This position requires working the 2nd shift from 2 PM to 10 PM, Monday through Friday, at the Eden Prairie site. You will spend the majority of your time on the manufacturing floor ensuring equipment runs efficiently and the area is properly cleaned. The role also involves desk work for reviewing batch records, writing protocols, and assisting with investigations. Initial training will be conducted on the 1st shift, Monday to Friday from 6 AM to 2 PM for two weeks. There may be opportunities for voluntary overtime on Saturdays and possibly Sundays. Job Type & Location This is a Contract to Hire position based out of Eden Prairie, MN. Pay and Benefits The pay range for this position is $26.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Eden Prairie,MN. Application Deadline This position is anticipated to close on Jun 26, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Associate Scientist-Benefits included. Job Description We are seeking a dedicated Associate Scientist to perform routine tests on various samples, including finished products, stability samples, and raw materials, using techniques such as UV and HPLC in a regulated laboratory environment. This role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution. Evaluate test results and determine the acceptability of samples based on the results. Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs. Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards. Review notebooks promptly and ensure compliance with SOPs. Analyze and interpret results in both written and oral formats. Assist in training new analysts. Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment. Required Skills Minimum 2 years of Experience in HPLC and Working in GMP Environment. Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master's degree with 1 year of experience. Problem-solving skills involving several concrete variables in standardized situations. Ability to perform necessary computations and interpret graphs. Working knowledge of instrumentation software used in laboratories. INTERESTED IN THIS ROLE? SEE BELOW TO BE IMMEDIATELY CONSIDERED: I am scheduling phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Fathima HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to fam or CALL- Job Type & Location This is a Contract to Hire position based out of Fort Lauderdale, FL. Pay and Benefits The pay range for this position is $29.00 - $39.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Jun 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Quality Scientist II Job Description The Quality Scientist II works within the Quality Department to support the testing and analysis of cGMP-produced viral vectors and cells. This role operates in a regulated GMP laboratory environment, performing and developing QC methods, supporting microbiological environmental monitoring, and maintaining high standards of documentation and compliance for cellular and gene therapy products. The position collaborates closely with Sr QC staff to help shape and implement strategic direction for the GMP area and contributes directly to the production of phase-appropriate clinical materials. Responsibilities Perform QC laboratory testing on cGMP-produced viral vectors and cells using techniques such as PCR, qPCR, ddPCR, gel electrophoresis, pH measurements, and related molecular biology assays. Support the development, optimization, and qualification of QC methods and assays under the guidance of experienced staff. Analyze microbiological environmental monitoring samples and document results in accordance with established procedures. Write, review, and revise Standard Operating Procedures (SOPs) to ensure they accurately reflect current laboratory practices and regulatory expectations. Perform routine equipment maintenance, monitoring, and basic troubleshooting to ensure laboratory instruments remain in a qualified and reliable state. Manage materials and supplies for QC and Production, including tracking inventory, coordinating replenishment, and ensuring appropriate storage and handling. Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the controlled manufacturing facility. Ensure all product samples are accurately labeled and that sample allocation, handling, and transfer are fully documented in the appropriate formats and systems. Maintain full accountability for product samples as they are distributed across different testing requirements and storage conditions. Evaluate processes related to sample management, identify gaps or inefficiencies, and implement improvements to enhance quality and throughput. Complete, review, file, and archive documentation according to SOPs and applicable regulatory requirements. Maintain compliance with regulatory requirements for cellular and gene therapy products through adherence to GMP, data integrity, and documentation standards. Perform daily work in accordance with established policies, procedures, and techniques, applying training and working knowledge to complete assigned tasks. Collaborate effectively in a diverse and team-oriented environment, using clear communication to support high productivity and shared goals. Document all activities performed in accordance with quality and regulatory expectations, ensuring accuracy, completeness, and traceability. Essential Skills Bachelor's degree (BS) in Biology or another relevant scientific discipline. Prior GMP laboratory experience, including familiarity with regulated documentation and quality systems. Hands-on experience performing molecular biology assays such as PCR, qPCR, and gel electrophoresis. Experience with assay execution and exposure to assay development activities. Strong understanding of regulatory and documentation requirements in a GMP environment, including data integrity and audit readiness. Ability to write, review, and follow SOPs and other controlled documents. Competence with basic laboratory techniques such as dilutions and pH measurements. Ability to work under close supervision while applying training and working knowledge to complete tasks accurately and efficiently. Strong attention to detail and organizational skills for sample management and documentation. Effective communication skills and the ability to work collaboratively within a cross-functional team. Additional Skills & Qualifications For a level II, seeking someone with 3+ years of gene therapy experience doing biological testing/assays . Would potentially consider candidates with less experience or even entry-level . Entry-level will need to have strong research experience where they were doing hands on biology or microbiology testing. In order to qualify as a Sci II, candidates must have either a Bachelors and 3+ years experience, or a Masters and 1+ years. Otherwise, they would be considered a Sci I. Work Environment The role is based in a new, state-of-the-art GMP facility with modern laboratories and equipment dedicated to the manufacture and testing of phase-appropriate materials, including viral vectors and cell-based products. The work environment is highly team-oriented, with close collaboration among a group of approximately 10-12 colleagues on each shift. The position is scheduled on first shift, Monday through Friday, generally from 8:00 a.m. to 4:30 p.m., with some flexibility as needed. The setting emphasizes strong communication, mutual support, and a culture that promotes growth and internal advancement. Dress code is business casual, appropriate for a professional laboratory environment. Job Type & Location This is a Contract to Hire position based out of Dublin, OH. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Dublin,OH. Application Deadline This position is anticipated to close on Jul 6, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: QA Analyst Job Description Join our team as a QA Analyst to ensure the success of our customers by maintaining quality through the auditing of the facility and production lines, evaluating raw materials, bulk, and finished products, and engaging in continuous improvement efforts. Responsibilities Perform reviews of Production Batch Records to maintain a world-class manufacturing control program, focusing on training and first-time right execution. Ensure documentation records are accurate and comply with GDP requirements. Ensure compliance with current SOPs, Work Instructions, and test procedures. Train personnel to improve compliance with regulatory and quality requirements. Provide technical and process direction and training to manufacturing personnel. Utilize interpersonal skills to help create a culture of quality and increase quality awareness. Document and investigate deviations and out-of-specification (OOS) situations. Ensure SOPs, Work Instructions, controlled forms, and test methods are proactively updated to support improvements and compliance. Ensure product quality specifications and customer standards are met and maintained to customer satisfaction. Complete approvals to run as needed and document quality events, such as deviations and non-conformances, for efficient decision-making. Ensure products meet specifications prior to release and maintain current reference and product standards. Accurately record data and pertinent information to focus improvement efforts that meet customer and regulatory requirements. Document OOS situations, determine root cause, and suggest solutions to prevent recurrence of issues. Maintain compliance with current regulatory expectations and practices, such as USP. Understand and maintain a culture of 'lean action' within the department to eliminate waste. Implement and maintain standards and processes that eliminate waste throughout the department. Apply and utilize 'lean tools' to permanently implement improvements. Institutionalize 5-S (Sort, Straighten, Shine, Standardize, and Sustain) in all aspects of the department. Essential Skills 1-2 years of experience in a GMP manufacturing environment such as pharmaceuticals, medical device, cosmetics, or food manufacturing. Experience reviewing batch records and/or compounding records. Bachelor's degree in Chemistry, Biology, or related field. Additional Skills & Qualifications Working knowledge of drug manufacturing regulations such as cGMP & 21CFR regulations. Experience with investigations & deviations. Attention to detail and ability to multi-task, verified by references. Strong sense of urgency and organization skills. Strong communication skills and confidence in enforcing policies. Demonstrates strong integrity and sound judgment. Work Environment This is a 2nd shift position from 2 PM to 10 PM, Monday through Friday, based at the Eden Prairie site. The role involves spending the majority of the time on the manufacturing floor, ensuring equipment efficiency and cleanliness. When not on the floor, duties include reviewing batch records, writing protocols, and assisting with investigations in a desk environment. Training on 1st shift will occur for two weeks, from 6 AM to 2 PM, Monday through Friday. Voluntary overtime may be available on Saturdays and possibly Sundays. The role offers exposure to a diverse manufacturing environment, including a wide range of products such as beauty, bath and body, lip balms, skincare, sunscreens, and cleaning detergents. The company experienced significant growth last year and anticipates continued expansion. Job Type & Location This is a Contract to Hire position based out of Eden Prairie, MN. Pay and Benefits The pay range for this position is $26.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Eden Prairie,MN. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: QC Scientist I (Bioassay) Job Description The QC Scientist I (Bioassay) supports Good Manufacturing Practice (GMP) manufacturing by performing analytical testing for commercial products and stability studies in a cGMP laboratory environment. You will use a range of analytical tools for large molecule analysis, including compendial methods, enzyme activity assays, and bioassays, to ensure timely and accurate testing of in-process, drug substance release, and stability samples. This role offers structured training, exposure to advanced analytical technologies, and the opportunity to grow within a collaborative, development-focused culture. Responsibilities Perform ELISA, compendial testing (pH, UV, osmolality, appearance), enzyme activity assays (including temperature and incubation parameters), and other bioassays on in-process, drug substance release, and stability samples to support GMP manufacturing and stability programs. Operate analytical instruments such as spectrometers, plate readers, and other minor laboratory equipment to execute assigned test methods accurately and efficiently. Conduct GMP testing in an analytical laboratory using HPLC and UPLC methods, including reverse phase, size-exclusion chromatography (SEC), concentration measurements, cation-exchange chromatography (CEX), and related techniques. Compile, analyze, and interpret test data, document results according to Standard Operating Procedures, and prepare clear and accurate reports. Review laboratory data packets as assigned to ensure completeness, accuracy, and compliance with applicable procedures and regulations. Perform and author laboratory investigations, including out-of-specification (OOS) and out-of-trend (OOT) assessments, as assigned by laboratory leadership. Recognize and promptly report invalid results, laboratory incidents, and out-of-specification or out-of-trend results to laboratory management, and recommend appropriate corrective actions or solutions. Contribute to the development and optimization of new analytical concepts, techniques, and standards to improve laboratory efficiency and data quality. Collaborate closely with team members, quality assurance, and data reviewers to ensure alignment, resolve issues, and maintain high-quality standards. Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and safety guidelines to maintain a compliant and safe laboratory environment. Participate in routine laboratory activities, including safety inspections, housekeeping, and ordering or managing laboratory supplies. Engage fully in the structured training program by successfully completing required testing qualifications on each method before progressing to additional assays. Essential Skills At least 1 year of proven experience working in a GMP regulated environment, including hands-on ELISA testing. Demonstrated experience performing compendial testing such as pH, UV, osmolality, and appearance measurements. Practical experience conducting enzyme activity assays, including control of temperature, incubation, and other critical parameters. Proficiency in operating spectrometers and plate readers for quantitative and qualitative analyses. Strong qualitative pipetting skills, including accurate and consistent pipetting technique. Ability to conduct GMP testing using HPLC and UPLC methods, including reverse phase, SEC, concentration measurements, and CEX, in an analytical laboratory setting. Working knowledge of EMPOWER or similar chromatography data systems and familiarity with MS Office and laboratory computer programs. Bachelor's degree in pharmaceutical sciences, biology, chemistry, biotechnology, or a related scientific field. Strong organizational and planning skills, with the ability to manage multiple tasks in a regulated environment. High attention to detail and accuracy in data recording, documentation, and review. Flexible, positive, and collaborative approach to working in a team-based laboratory setting. Additional Skills & Qualifications Experience with SoloVPE for concentration or related measurements. Familiarity with qPCR techniques and workflows. Hands-on experience with colorimetric assays such as Picogreen and Bradford. Experience working with 96-well plates and multi-channel pipettes for high-throughput testing. Exposure to peer data review processes in a quality control environment. Experience conducting or contributing to investigations, including out-of-specification (OOS) and out-of-trend (OOT) assessments. Experience in quality control, wet chemistry, bioassays, and UV-Vis analytical techniques. Strong general computer literacy and comfort working with laboratory information and documentation systems. Demonstrated ability to adapt to changing priorities and learn new methods and technologies quickly. Work Environment This position is based in a pharmaceutical quality control laboratory where you will perform bench-level analytical work in a cGMP-compliant setting. The role includes an intensive training period of approximately 3 to 6 months, during which you will qualify on each test method before progressing to additional assays. You will work Monday through Friday with a standard daytime schedule and a flexible start time around typical business hours. The environment is highly regulated and safety-focused, with established Standard Operating Procedures, Good Manufacturing Practices, and safety guidelines governing daily activities. You will have access to modern analytical equipment, including HPLC, UPLC, spectrometers, plate readers, and related bioanalytical tools. The culture emphasizes continual growth, learning, and empowerment, with opportunities to convert to a full-time role based on performance and to contribute meaningfully to advancing pharmaceutical products. Job Type & Location This is a Contract to Hire position based out of Berkeley, MO. Pay and Benefits The pay range for this position is $28.00 - $31.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Berkeley,MO. Application Deadline This position is anticipated to close on Jul 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: CNC Programmer Job Description We are seeking a skilled CNC Programmer in Streator, IL to take full ownership of offline programming for a modern machining environment. In this role, you will develop, optimize, and maintain CNC programs for mills and lathes, with a strong focus on efficiency, accuracy, and problem-solving. You will serve as the primary programming resource, supporting production by creating and refining programs, collaborating with operators, and contributing to continuous improvement across the shop. Responsibilities Create, edit, and maintain offline CNC programs for 3-axis mills and Haas lathes with live tooling using G & M code and programming software such as Mastercam. Program bar feeders and related automation to support efficient, continuous production. Translate engineering drawings, models, and process requirements into effective CNC programs that meet quality and productivity targets. Optimize tool paths, cutting parameters, and setups to reduce cycle times, improve tool life, and enhance overall machining efficiency. Collaborate with CNC operators on the shop floor to support new part introductions, troubleshoot issues, and make program tweaks directly at the machines when needed. Perform and support machine setups to ensure programs run correctly and safely on mills and lathes. Act as the primary owner of all offline CNC programming activities, ensuring programs are organized, documented, and updated as processes evolve. Work closely with manufacturing engineering to identify and implement process improvements and more efficient machining strategies. Assist in diagnosing and resolving machining and programming problems, serving as a key problem solver for complex parts and operations. Provide guidance and, where possible, training to CNC operators to help them better understand programs, setups, and best practices. Maintain a strong focus on safety, quality, and consistency in all programming and machining activities. Essential Skills Proven experience in CNC programming, with a strong focus on offline programming for mills and lathes. Hands-on experience programming 3-axis mills and Haas lathes with live tooling. Proficiency in G & M code programming for CNC machines. Experience using Mastercam or similar CAD/CAM software for offline CNC programming. Ability to develop and optimize CNC programs for bar feeders and related automation. Strong understanding of CNC setups, including tooling, workholding, and machine offsets. High school diploma or equivalent. Ability to troubleshoot machining and programming issues and implement effective solutions. Strong problem-solving mindset and a continuous improvement approach to machining processes. Effective communication skills to work with operators, engineers, and other team members on the shop floor. Additional Skills & Qualifications Experience training or mentoring CNC operators on programming concepts, setups, or best practices. Experience as a CNC machinist with programming responsibilities. Ability to collaborate with manufacturing engineering to drive process improvements and efficiency gains. Comfort working as the primary or sole CNC programmer responsible for offline programming in a production environment. Work Environment This role operates in a production machining environment equipped with 3-axis mills and Haas lathes featuring live tooling, as well as bar feeders and related automation. The majority of the work-approximately 80-90%-takes place in an office or programming area, focused on offline CNC programming using tools such as Mastercam and G & M code. You may occasionally work on the shop floor alongside CNC operators to support new part setups, troubleshoot issues, or fine-tune programs at the machine. The environment emphasizes efficiency, problem-solving, and collaboration between programming and operations, with a strong focus on safe, consistent, and high-quality machining. Job Type & Location This is a Contract to Hire position based out of Streator, IL. Pay and Benefits The pay range for this position is $35.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Streator,IL. Application Deadline This position is anticipated to close on Jun 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: Production Scientist Job Description The Production Scientist supports early-phase development of Active Pharmaceutical Ingredients (APIs) by synthesizing small organic molecules and API-related impurities. In this role, you collaborate closely with lead research scientists to manufacture new and existing products during process development, optimization, technology transfer, scale-up, and process validation activities. You apply strong chemistry knowledge, follow current Good Manufacturing Practices (cGMP), and communicate effectively with multidisciplinary teams while contributing to high-quality, timely project delivery. Responsibilities Perform chemical reactions on scales ranging from gram to multi-kilogram quantities to support API development and manufacturing. Execute chemical synthesis, isolation, and related laboratory tasks while maintaining strict attention to detail to meet safety, quality, schedule, and customer objectives. Operate manufacturing and laboratory equipment safely and productively in accordance with established procedures. Recognize processing and quality issues during production and promptly escalate concerns to project leads or appropriate team members. Read, understand, and comply with technical documents, batch records, and standard operating procedures. Perform accurate calculations using simple mathematical formulas and operations to support laboratory and manufacturing activities. Record experimental and production results in a neat, precise, and compliant manner following cGMP and other applicable regulations. Carry out equipment qualification, calibration, maintenance, and cleaning activities as required to ensure reliable and compliant operation. Assist with data entry, document drafting, and other laboratory documentation tasks to support project and regulatory requirements. Complete all required cGMP and other relevant company training in a timely manner and apply this knowledge in daily work. Collaborate with lead research scientists and cross-functional teams during process development, optimization, technology transfer, scale-up, and process validation. Support API and API-related impurity synthesis and testing in alignment with customer needs and project goals. Essential Skills Strong chemistry background with hands-on experience in chemical synthesis of small organic molecules. Experience performing Active Pharmaceutical Ingredient (API) testing and API-related analytical work. Familiarity with current Good Manufacturing Practices (cGMP) and previous experience in a GMP-regulated environment, or successful completion of a GMP class as a substitute. Ability to conduct and monitor chemical reactions from gram to multi-kilogram scale safely and effectively. Proficiency in applying a full suite of analytical testing techniques to support chemistry and API testing. Capability to read, interpret, and follow technical documents, batch records, and standard operating procedures accurately. Strong attention to detail with the ability to maintain high standards of data integrity and documentation under cGMP. Competence in performing basic mathematical calculations required for laboratory and manufacturing tasks. Effective written communication skills for documenting work and contributing to technical documents. Ability to collaborate in a diverse, multidisciplinary team environment. Additional Skills & Qualifications Experience working in a contract development and manufacturing organization (CDMO) or similar environment supporting multiple external customers. Exposure to process development, optimization, technology transfer, scale-up, or process validation activities for APIs. Comfort working with a wide variety of pharmaceutical customers and adapting to different project requirements. Strong organizational skills and the ability to manage multiple tasks while meeting project timelines. Demonstrated commitment to ongoing training and professional development in cGMP and pharmaceutical manufacturing practices. Work Environment This is an on-site role within a dedicated laboratory and manufacturing environment as part of a smaller team of approximately 30-40 people. You work normal business hours, typically Monday through Friday from 8:00 a.m. to 5:00 p.m., with some flexibility as needed to support project timelines. The facility operates as a contract development and manufacturing organization (CDMO) that partners with a wide variety of mid-size to large pharmaceutical companies on their API pipeline. You will work in a regulated cGMP setting, using standard laboratory and manufacturing equipment for chemical synthesis, analytical testing, and API production, and you follow appropriate laboratory safety practices and attire suitable for a GMP laboratory environment. Job Type & Location This is a Contract position based out of Cary, NC. Pay and Benefits The pay range for this position is $30.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Cary,NC. Application Deadline This position is anticipated to close on Jul 9, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Description -Will be working doing bench testing which includes; -Sample prep -Wet Chemistry -Standard weighs -Dilutions -And over time will be trained on HPLC and GC Will be trained in both the Oral Dose Solids and Nasals departments. Conducts chemical and physical analyses in support of the development of a manufacturable multisource pharmaceutical product. Provides analytical support for the release of registration materials in support of regulatory submissions. Assists analytical method validation and transfer activities. Performs the assigned analytical tasks in support of product development, registration lot release, pre and post regulatory submission activities. Performs activities within the assigned timelines and in compliance with cGXP's, and company practices and procedures. Follows work instructions, SOPs and company practices. Documents analytical activities and results accurately, in a timely manner and right-first time and maintains integrity of data. Follows written analytical procedures. Identifies execution challenges of analytical methods and support trouble shooting activities. Skills Dilutions, sample preparation, biochemistry, Quality control, Chemistry, Hplc, Chemical Testing Top Skills Details Dilutions, sample preparation, biochemistry,Quality control,Chemistry,Hplc Additional Skills & Qualifications MUST - Bachelors in Science Field Prefer candidates with Bachelors in Chemistry or Biochemistry but will look at candidates with Biology, Microbiology, Physics, Enviornmental Science, Pharmaceutical Science but must have strong Chem lab experience from school or outside of school Must have prior lab experience but can be from school Strongly prefer candidates that have lab experience outside of academia Must be able to work in a team environment approach to accomplish tasks assigned. Must possess the ability to work on multiple tasks in a fast pace environment. Must possess good written and verbal communication skills. The candidate must have the ability to work with supervision using scientific judgment and professional competency. Experience Level Entry Level Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Jul 6, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: CNC Programmer Job Description We are seeking a skilled CNC Programmer in Streator, IL to take full ownership of offline programming for a modern machining environment. In this role, you will develop, optimize, and maintain CNC programs for mills and lathes, with a strong focus on efficiency, accuracy, and problem-solving. You will serve as the primary programming resource, supporting production by creating and refining programs, collaborating with operators, and contributing to continuous improvement across the shop. Responsibilities Create, edit, and maintain offline CNC programs for 3-axis mills and Haas lathes with live tooling using G & M code and programming software such as Mastercam. Program bar feeders and related automation to support efficient, continuous production. Translate engineering drawings, models, and process requirements into effective CNC programs that meet quality and productivity targets. Optimize tool paths, cutting parameters, and setups to reduce cycle times, improve tool life, and enhance overall machining efficiency. Collaborate with CNC operators on the shop floor to support new part introductions, troubleshoot issues, and make program tweaks directly at the machines when needed. Perform and support machine setups to ensure programs run correctly and safely on mills and lathes. Act as the primary owner of all offline CNC programming activities, ensuring programs are organized, documented, and updated as processes evolve. Work closely with manufacturing engineering to identify and implement process improvements and more efficient machining strategies. Assist in diagnosing and resolving machining and programming problems, serving as a key problem solver for complex parts and operations. Provide guidance and, where possible, training to CNC operators to help them better understand programs, setups, and best practices. Maintain a strong focus on safety, quality, and consistency in all programming and machining activities. Essential Skills Proven experience in CNC programming, with a strong focus on offline programming for mills and lathes. Hands-on experience programming 3-axis mills and Haas lathes with live tooling. Proficiency in G & M code programming for CNC machines. Experience using Mastercam or similar CAD/CAM software for offline CNC programming. Ability to develop and optimize CNC programs for bar feeders and related automation. Strong understanding of CNC setups, including tooling, workholding, and machine offsets. High school diploma or equivalent. Ability to troubleshoot machining and programming issues and implement effective solutions. Strong problem-solving mindset and a continuous improvement approach to machining processes. Effective communication skills to work with operators, engineers, and other team members on the shop floor. Additional Skills & Qualifications Experience training or mentoring CNC operators on programming concepts, setups, or best practices. Experience as a CNC machinist with programming responsibilities. Ability to collaborate with manufacturing engineering to drive process improvements and efficiency gains. Comfort working as the primary or sole CNC programmer responsible for offline programming in a production environment. Work Environment This role operates in a production machining environment equipped with 3-axis mills and Haas lathes featuring live tooling, as well as bar feeders and related automation. The majority of the work-approximately 80-90%-takes place in an office or programming area, focused on offline CNC programming using tools such as Mastercam and G & M code. You may occasionally work on the shop floor alongside CNC operators to support new part setups, troubleshoot issues, or fine-tune programs at the machine. The environment emphasizes efficiency, problem-solving, and collaboration between programming and operations, with a strong focus on safe, consistent, and high-quality machining. Job Type & Location This is a Contract to Hire position based out of Peru, IL. Pay and Benefits The pay range for this position is $35.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Peru,IL. Application Deadline This position is anticipated to close on Jun 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: Engineering Technician - Oil & Gas Job Description Support project by executing chemical and petroleum lab scale experiments. Build up test equipment, compile, and report test data. Work with engineers to generate mass balances and data compilations. Perform sample collection and equipment maintenance/troubleshooting. Training provided by a chemist or lead engineer. Responsibilities Execute chemical and petroleum lab scale experiments. Build and modify test equipment as needed. Compile and report test data. Collaborate with engineers to generate mass balances and data compilations. Perform sample collection. Maintain, troubleshoot, and repair instrumentation, mechanical, and electrical equipment. Assist in the safe start-up, operation, and shutdown of plant equipment. Inspect equipment at periodic intervals to detect malfunctions or need for repair. Monitor plant air and water emissions. Support plant operations using SCADA software, with training provided. Essential Skills Mechanical aptitude Ability to read AutoCAD drawings Proficiency in MS Office, particularly Excel Experience with tubing and pipe-fittings Understanding of basic fluid flow and gas flow and pressure Additional Skills & Qualifications High School Diploma Experience in board operations is preferred Willingness to work overtime and shift work Pay rate- $25-32 based on expereince Board operations is a plus Work Environment Work in a research and development setting with innovative process development. The role involves both inside and outside work. Training will be provided for operations with SCADA software. Candidates must be willing to adapt to a dynamic work environment that includes shift work. Job Type & Location This is a Contract position based out of San Antonio, TX. Pay and Benefits The pay range for this position is $22.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Antonio,TX. Application Deadline This position is anticipated to close on Jul 7, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Actalent is hiring for an Associate Scientist (Analytical Development) in the Thousand Oaks area! Location: Fully Onsite Schedule: Standard business hours Experience Level: Intermediate About the Role We are seeking an Associate Scientist to support analytical development efforts for biotherapeutic drug products. This role focuses on performing analytical testing to evaluate key product attributes and generate data that informs critical development decisions. You will collaborate with cross-functional teams to assess biochemical and biophysical characteristics and contribute to advancing product development through high-quality data and insights. Key Responsibilities Perform analytical testing to evaluate attributes of biotherapeutic drug products Execute and support development of analytical methods to assess product quality and performance Analyze experimental data and provide clear, actionable insights to project teams Document experimental procedures, results, and conclusions in accordance with established standards Collaborate with cross-functional teams to support drug product development and advancement Maintain laboratory equipment and ensure compliance with safety and operational procedures Required Qualifications Bachelor's or Master's degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field Minimum 2+ years of industry or relevant laboratory experience Hands-on experience with analytical assays Strong experimental lab skills and data analysis capabilities Preferred Qualifications Experience with mass spectrometry Familiarity with analytical techniques used to assess biotherapeutic products Key Skills & Competencies Strong critical thinking and data interpretation skills High level of attention to detail and documentation accuracy Ability to work effectively in a team-oriented environment Solid foundation in analytical chemistry techniques Effective communication skills for sharing data and insights Work Environment This role is based in a laboratory setting and requires hands-on experimental work in support of analytical development activities. Job Type & Location This is a Contract position based out of Thousand Oaks, CA. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Thousand Oaks,CA. Application Deadline This position is anticipated to close on Jul 7, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description About the Role As an Engineer Technician II , you'll gain hands on exposure to engineering projects that support critical power and utility infrastructure. This entry level role is perfect for someone eager to learn, work in both the field and the office, and build a strong technical foundation alongside experienced engineers. You'll support engineering design, data collection, field inspections, and construction activities-playing a meaningful role in projects that keep communities connected and powered. What You'll Do Collect, analyze, and organize technical data to support engineering and design efforts Assist with engineering documentation including drawings, diagrams, reports, and schematics Perform basic engineering calculations and data analysis following established standards Support field inspections, site visits, and data collection at active project locations Help set up and execute tests, document results, and assist with engineering evaluations Support construction activities and participate in post construction compliance reviews Assist with root cause analysis of outages and help develop mitigation strategies Coordinate with internal teams and external partners such as permitting agencies and right of way specialists Transition field data into office based design work and electrical work packages What You Bring High school diploma or equivalent Associate's or Bachelor's degree in Engineering Technology (or related discipline) Fundamental understanding of basic scientific and engineering principles Strong math skills and attention to detail Proficiency with Microsoft Word, Excel, and Outlook Ability to work both indoors and outdoors in support of project needs Strong communication skills and a collaborative mindset Willingness to learn, take direction, and grow under close supervision Nice to Have (Not Required) Exposure to power, utilities, or infrastructure projects Experience with field data collection or construction support Familiarity with permitting, right of way coordination, or outage analysis Why You'll Love This Role Hands on experience in both field and office engineering environments Mentorship from experienced engineers and project leaders Opportunity to build real world skills that accelerate your engineering career Work on projects that directly support critical power and utility systems A collaborative, team focused environment where learning is encouraged Work Environment This role offers a dynamic mix of office based technical work and field assignments. You'll collaborate with engineers, construction teams, and external stakeholders while gaining exposure to the full lifecycle of engineering and utility projects. Job Type & Location This is a Contract to Hire position based out of Atlanta, GA. Pay and Benefits The pay range for this position is $26.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Atlanta,GA. Application Deadline This position is anticipated to close on Jul 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Description The Engineering Technician supports the engineering team in the design, development, validation, and continuous improvement of safety-critical products. This role assembles product samples and prototypes, assists with test execution and process inspections, and supports prototype tooling setup and installation. The Engineering Technician contributes directly to quality assurance testing and validation of process changes in a fast-paced manufacturing environment where the products have a meaningful impact on people's lives. Responsibilities Support the engineering team in the design, development, validation, and improvement of products. Assemble product samples, prototypes, and test fixtures with a high level of mechanical accuracy. Assist with test execution, including setup, operation, and monitoring of tests according to engineering instructions. Perform process inspections and support validation activities to ensure products meet established specifications and standards. Support prototype tooling setup and installation to enable new product and process development. Contribute to quality assurance testing and validation of process changes by following defined procedures and documenting results. Use measurement and inspection tools such as calipers, micrometers, and gauges to verify dimensions and tolerances. Read and interpret engineering drawings, specifications, and work instructions to carry out build and test activities. Collect, record, and organize test and inspection data, and prepare basic reports using tools such as Excel and Word or equivalent software. Troubleshoot basic mechanical and process issues during assembly, testing, or inspection and communicate findings to the engineering team. Follow metrology and calibration practices to ensure measurement tools remain accurate and reliable. Skills & Qualifications 2+ years of hands-on experience in a manufacturing, testing, or engineering support environment. Working knowledge of manufacturing processes, materials, and basic engineering principles. Ability to read and interpret engineering drawings, specifications, and work instructions. Proficiency with basic measurement and inspection tools, including calipers, micrometers, and gauges. Experience with data collection, documentation, and basic reporting using Excel, Word, or equivalent software. Mechanical aptitude with hands-on experience assembling products, prototypes, or test fixtures. Experience performing or supporting quality assurance, metrology, calibration, and troubleshooting activities. Strong attention to detail and accuracy in measurement, documentation, and assembly work. Ability to operate effectively in a fast-paced environment with evolving or not fully defined processes. Nice to Have Associate degree or technical certification in engineering technology, manufacturing, or related field Experience supporting product testing, validation, or quality inspection activities Military experience Job Type & Location This is a Contract to Hire position based out of Cleveland, OH. Pay and Benefits The pay range for this position is $27.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Cleveland,OH. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: Traveling Superintendent Job Description This Traveling Superintendent role oversees mission critical and data center construction projects across the United States, from preconstruction through commissioning and final turnover. You will lead field operations, coordinate complex MEP and critical systems installations, and ensure safe, high-quality execution in active and operational facilities. The position requires extensive travel, strong communication and leadership skills, and the ability to manage multiple stakeholders while maintaining schedule, safety, and operational reliability. Responsibilities Participate in project kickoff meetings with project executives and teams to understand project goals, critical systems requirements, commissioning milestones, client expectations, and operational constraints. Host field kickoff meetings with trade partners, commissioning agents, vendors, and project managers to align on scope, schedule, and critical systems execution. Manage day-to-day relationships with trade partners and vendors, with a strong focus on critical systems installation, startup, testing, and turnover. Manage relationships between site teams, facility operators, client representatives, commissioning teams, and ownership groups to maintain alignment and clear communication. Participate in project closeout meetings and provide feedback on trade partner performance, quality, commissioning readiness, and turnover execution. Host trade partner gatherings for project closeout and lessons learned to drive continuous improvement. Lead weekly on-site toolbox talks with all trade partners and document these meetings in Procore. Lead weekly on-site foremen meetings to review 3-week lookaheads, commissioning activities, constraints, shutdowns, and critical path items. Essential Skills 5-15+ years of experience as a Superintendent with significant experience delivering mission critical, data center, high-tech, or complex MEP-intensive projects. Proven experience managing mission critical projects from preconstruction through commissioning, turnover, and operational readiness, including sitework, structural work, major MEP systems, and critical equipment installation. Demonstrated experience coordinating critical electrical infrastructure including switchgear, UPS systems, generators, PDUs, and associated distribution systems. Demonstrated experience coordinating critical mechanical infrastructure including cooling systems, chilled water systems, CRAH/CRAC units, controls, and building automation systems. Strong understanding of commissioning processes, startup procedures, integrated systems testing, turnover requirements, and outage management protocols within active mission critical environments. Experience working within active data centers or operational facilities with strict uptime requirements (preferred but highly relevant). Strong professional communication skills with clients, design teams, commissioning agents, trade partners, facility operators, and internal stakeholders. Demonstrated proactive problem-solving skills, including early identification of design, constructability, and coordination issues during preconstruction and active construction phases. Comfort leading field meetings, toolbox talks, and coordination sessions with multiple trades and stakeholders. Ability to work flexible schedules and weekends, along with extended stays away from home, to support project needs. Comfort using construction management technology platforms such as Procore and Sway for documentation, reporting, and communication. Ability to create and manage 3-week lookaheads in Outbuild or similar scheduling tools. Strong organizational skills to manage documentation, schedules, field tickets, RFIs, and commissioning records on complex projects. Commitment to maintaining a strong safety culture and adherence to safety protocols on active and mission critical sites. Additional Skills & Qualifications Experience on projects of $1M+ in construction value. Experience supporting or leading projects across sectors such as workplace, amenity, retail, hospitality, healthcare, lab and life sciences, and education (a plus). Comfortable representing the company in client presentations, interviews, and pursuit efforts. Ability to mentor, coach, and support junior field staff, contributing to a consistent traveling superintendent culture. No formal degree, software, or certification requirements; candidates without OSHA 30 will be sponsored to complete it. Interest in working within a collaborative, high-accountability environment that values empathy, integrity, perseverance, and curiosity. Willingness to contribute to continuous improvement by sharing lessons learned and feedback at project closeout. Job Type & Location This is a Permanent position based out of Chicago, IL. Pay and Benefits The pay range for this position is $110000.00 - $200000.00/yr. Travel Package: - $80 per diem per work day - pay for hotel and airfare - expense gas/essentials - offer company card as well Gold PPO Health Insurance 401k Plan Unlimited Flex PTO Commuter Benefits, Paid Family Leave Professional Development Volunteer Time Off Workplace Type This is a fully onsite position in Chicago,IL. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: Site Safety and Health Officer (SSHO) - Great Lakes Job Description This role serves as the full-time on-site Site Safety and Health Officer (SSHO) for a federal construction project, ensuring strict adherence to safety and compliance standards. The SSHO oversees implementation of the Accident Prevention Plan, enforces applicable regulations, and acts as the designated Competent Person for multiple high-risk activities. The position focuses on construction safety, regulatory compliance, and proactive risk management on a major roof replacement project at a federal health care facility. Responsibilities Serve as the full-time on-site Site Safety and Health Officer (SSHO) during all construction activities. Ensure full compliance with 29 CFR 1926, EM 385-1-1, OSHA, and all applicable federal, state, and local safety regulations. Implement, administer, and continuously monitor the project-specific Accident Prevention Plan (APP). Act as the designated Competent Person for fall protection, including oversight of systems, equipment, and work practices. Act as the designated Competent Person for excavation and trenching activities, including inspections and hazard controls. Act as the designated Competent Person for scaffolds and ladders, ensuring proper setup, use, and inspection. Act as the designated Competent Person for rigging and crane operations, verifying safe practices and compliance. Act as the designated Competent Person for fire and life safety, including emergency procedures and prevention measures. Provide qualified alternate safety coverage when temporarily off-site, ensuring continuous safety oversight. Conduct site safety inspections and audits to identify hazards and verify compliance with safety requirements. Coordinate and deliver safety training and toolbox talks for construction personnel as needed. Support and document incident investigations, near-miss reporting, and corrective actions. Collaborate with project stakeholders to integrate safety requirements into planning and daily operations. Maintain accurate safety records, logs, and documentation required by project and regulatory standards. Essential Skills Demonstrated experience in construction safety on active job sites. Strong knowledge of OSHA construction standards, including 29 CFR 1926. In-depth understanding of EM 385-1-1 requirements and their application to federal construction projects. Proven ability to implement and administer project-specific Accident Prevention Plans (APPs). Competence in overseeing fall protection, excavation and trenching, scaffolds and ladders, rigging and cranes, and fire and life safety. OSHA 30-Hour Construction Safety training completed within the last 5 years. Either a minimum of 7+ years of construction safety experience, or a Safety & Health degree plus 5+ years of construction safety experience. Ability to provide safety training and promote a strong health and safety culture on site. Experience working on federal construction projects or similar highly regulated environments. Capability to interpret and apply safety regulations at the federal, state, and local levels. Strong communication skills to effectively interact with site personnel and project stakeholders. Attention to detail and thoroughness in inspections, documentation, and compliance activities. Additional Skills & Qualifications Current professional safety certification is preferred. Experience as a Site Safety and Health Officer (SSHO) on commercial or federal construction projects. Background in health and safety compliance, including safety training and incident prevention programs. Familiarity with construction activities related to roofing and work on occupied facilities. Ability to coordinate with multiple agencies and stakeholders on federal projects. Strong organizational skills to manage documentation, reporting, and multiple safety responsibilities. Comfort working as a designated Competent Person across multiple scopes of work. Work Environment The role is based on a construction project to replace the roof on a main hospital within a federal health care center. The environment involves active construction operations in and around a functioning medical facility, requiring heightened awareness of patient care activities and strict adherence to safety and access controls. Work is performed on a federal construction site governed by EM 385-1-1 and OSHA standards, with frequent exposure to outdoor conditions, elevated work areas, and typical construction hazards such as noise, dust, and equipment movement. The position requires regular presence on scaffolds, ladders, and roof surfaces, as well as in areas where cranes, rigging, and other heavy construction equipment operate. The SSHO collaborates closely with federal agencies and project stakeholders in a structured, compliance-driven setting. Appropriate personal protective equipment (PPE) is required at all times in accordance with site safety policies. Job Type & Location This is a Contract position based out of North Chicago, IL. Pay and Benefits The pay range for this position is $40.87 - $48.07/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in North Chicago,IL. Application Deadline This position is anticipated to close on Jul 7, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Hiring for an Engineering Technician in East Hartford, CT Job Description The Engineering Technician provides technical and administrative support to a Non-Destructive Evaluation (NDE) engineering team, helping to develop and implement universal inspection methods for aerospace parts. This role supports the processing and delivery of inspection tools, assists with analysis of NDE data, and tracks inspector assignments and progress for both commercial and military engines. The position involves hands-on preparation and post-inspection handling of parts, coordination with vendors, and documentation of inspection activities, while contributing to cutting-edge research and development in aerospace safety. Responsibilities Provide technical and administrative support to the NDE engineering team to facilitate processing and delivery of inspection tools and analysis of NDE data. Coordinate inspection assignments, schedule inspectors, and track progress and completion of inspection results. Request and obtain quotes from vendors, monitor order status against schedule requirements, and verify that all technical and quality requirements are met upon delivery. Perform technical and inventory activities under the direction of NDE Engineers to support commercial and military engine programs. Prepare parts for fluorescent penetrant inspection (FPI), including cleaning, handling, and proper identification according to established procedures. Clean parts after inspection and ensure they are properly packaged, labeled, and stored or shipped in accordance with inspection and quality requirements. Prepare, maintain, and organize inspection documentation, ensuring accuracy, completeness, and traceability of records. Proctor inspector qualifications and assessments, including overseeing test sessions and ensuring adherence to established procedures. Travel approximately 20-30% of the time to qualify inspector locations and support NDE activities at various sites. Support and help refine non-destructive evaluation methods such as eddy current, ultrasonic, and borescope techniques within an R&D laboratory environment. Assist in establishing and maintaining NDT and general quality systems and methods, including documentation and process adherence. Apply knowledge of aerospace manufacturing operations to support inspection planning, execution, and continuous improvement. Use root cause and process control tools to help identify issues, support corrective actions, and improve inspection processes. Communicate effectively with all levels of management, internal stakeholders, and external customers to provide updates, clarify requirements, and resolve issues. Utilize SAP and the Microsoft Office suite, including Excel, to manage data, track assignments, generate reports, and maintain records. Maintain strong organization of tasks, documentation, and inventory to support a dynamic environment with frequently changing priorities. Work independently when required, managing time and tasks to meet core hours and project deadlines. Essential Skills Associate Degree in Technology or Bachelor of Technology, with an Engineering Technology (ET) focus preferred. Experience establishing non-destructive testing (NDT) and general quality systems and NDT methods. Knowledge of aerospace manufacturing operations and related inspection requirements. Proficiency in Microsoft Excel for data tracking, reporting, and analysis. Experience with SAP and the broader Microsoft Office suite. Strong written and verbal communication skills, with the ability to communicate effectively with all levels of management and with internal and external customers. Excellent organizational skills and the ability to manage multiple tasks in a dynamic environment. Ability to work independently and take ownership of assigned responsibilities. Knowledge and experience with root cause analysis and process control tools. Familiarity with electronics, electrical concepts, test equipment, and blueprint reading to support NDE activities. Additional Skills & Qualifications Associate of Science in Engineering Technology (ASET) or similar technical degree preferred. Background in non-destructive evaluation methods such as eddy current, ultrasonic, and borescope techniques. Experience preparing parts for fluorescent penetrant inspection (FPI) and performing post-inspection cleaning and packaging. Prior exposure to aerospace engines, including commercial and military applications. Demonstrated ability to thrive in a structured, process-driven organization. Experience coordinating with vendors, including requesting quotes, tracking orders, and verifying requirements upon delivery. Strong attention to detail and commitment to quality, particularly in safety-critical aerospace applications. Interest in working on flight safety problems and contributing to advanced aerospace R&D initiatives. Work Environment This role is based full-time onsite at a campus in East Hartford within a dynamic R&D laboratory group focused on non-destructive evaluation of aerospace parts. The team operates in a fast-paced environment where priorities can change frequently, requiring flexibility and strong organizational skills. The work involves hands-on interaction with aerospace components, test equipment, and inspection tools, including methods such as eddy current, ultrasonic, borescope, and fluorescent penetrant inspection. You will use SAP and Microsoft Office tools, particularly Excel, as part of daily responsibilities. The schedule offers flexible start and stop times as long as core hours are fulfilled. The position may require travel approximately 20-30% of the time to qualify inspector locations and support offsite activities. The culture emphasizes structure, process discipline, and continuous improvement, with a focus on solving flight safety problems and advancing cutting-edge aerospace technologies. There is potential for conversion to a permanent role, and the contract period includes paid time off, paid holidays, and overtime opportunities at a premium rate for hours worked over 40 per week. Job Type & Location This is a Contract position based out of East Hartford, CT. Pay and Benefits The pay range for this position is $26.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in East Hartford,CT. Application Deadline This position is anticipated to close on Jul 7, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Engineering TechnicianPosition Overview The Engineering Technician supports mechanical testing, verification, and laboratory activities for ventilator hardware and related systems at a medical device research and development site. This is a hands on, mid level technician role, ideal for someone who enjoys working in labs and machine shops, has a strong understanding of pneumatics, and thrives in a fast paced, highly collaborative engineering environment. This position is not an engineering role and not entry level. The technician works closely with engineers to build and modify test fixtures, execute detailed test plans, troubleshoot mechanical and pneumatic systems, and support verification activities through machining, fabrication, and test execution. Key Responsibilities Build, integrate, and modify mechanical and pneumatic test fixtures to support engineering verification and validation test plans. Execute a wide range of mechanical and environmental tests, including: Pool and water tests Shock and vibration testing Environmental and temperature testing Mechanical verification testing Perform extensive hands on pneumatic work, including: Building integrated pneumatic test fixtures Assembling and routing complete pneumatic circuits Troubleshooting pneumatic systems used in testing Support test setup and troubleshooting for complex mechanical assemblies and high reliability hardware. Operate CNC machines for light machining and fabrication tasks; CNC programming experience is a plus but not required. Perform manual machining using standard shop equipment, including work with sheet metal, small parts, manifolds, fittings, and related hardware. Wire and integrate test fixtures, including basic electronics assembly and connections to test equipment. Run tests and perform basic calibration of test equipment and fixtures following established procedures. Build and verify test setups using engineering drawings, schematics, wiring diagrams, and written instructions. Execute engineer provided test plans accurately and consistently, with clear documentation of results. Support lab activities related to design changes, verification testing, and development of custom test fixtures. Set up, execute, and document shock and vibration tests, supporting analysis activities as needed. Use ERP systems and documentation tools (including Visio where applicable) to track fixtures, configurations, and test activities. Collaborate with engineers and fellow technicians to resolve test issues and suggest practical improvements to fixtures and setups. Work 100% onsite and support a multi year contract environment, maintaining a strong focus on quality, safety, and reliability. Required Skills & Experience Strong mechanical aptitude with demonstrated, hands on experience in a lab or shop environment. Minimum 2+ years of relevant technician experience; 3+ years strongly preferred. Hands on experience wiring and integrating mechanical and pneumatic test fixtures. Proven ability to troubleshoot complex mechanical assemblies and test setups. Experience working with sheet metal and small hardware components such as manifolds, chambers, fittings, and related parts. Ability to execute tests and perform basic calibration of test equipment. Experience building complete pneumatic circuits from drawings and integrating them into test fixtures. Required experience operating CNC machines; programming experience is beneficial but not mandatory. Manual machining experience using standard shop tools and equipment. Ability to read and work from engineering drawings, schematics, wiring diagrams, and written procedures. Familiarity with pneumatics, test equipment, electronics assembly, and basic wiring practices. Willingness and ability to work 100% onsite. Commitment to a 2 year contract role. This position is not open to recent graduates and requires prior practical, hands on experience. Preferred Qualifications Experience with environmental chamber testing (training can be provided if needed). Background in aerospace, industrial, or other high reliability hardware environments. Exposure to ventilators or other complex mechanical and electro mechanical systems. Experience using SolidWorks or similar CAD tools to understand fixtures and assemblies. Familiarity with ERP systems for tracking work orders, parts, and test activities. Experience using Visio or similar tools for diagrams and process flows. Experience setting up and executing pool and water tests in controlled environments. Knowledge of shock and vibration testing methods and analysis. Strong attention to detail and documentation skills. Ability to collaborate effectively with engineers and technicians in a fast moving R&D setting. Work Environment This role is based at a medical device research and development facility focused on ventilator hardware and related life support systems. Work is performed entirely onsite in a lab and shop environment that combines mechanical, pneumatic, and basic electronic testing. The facility includes test laboratories, environmental chambers, shock and vibration equipment, pool and water test setups, and dedicated areas for mechanical verification. Daily work involves CNC machines, manual machining equipment, sheet metal tools, and standard hand and power tools. Test equipment includes pneumatic test systems, calibration tools, environmental rigs, and electronic instrumentation. The environment is fast paced and collaborative, with close interaction between technicians and engineers. Safety, precision, quality, and documentation are core expectations, supported by structured test plans, engineering drawings, ERP systems, and formal procedures. About the Company This organization is a global leader in medical technology, dedicated to improving outcomes for patients facing critical and life threatening conditions. With decades of experience developing high reliability medical devices, the company is known for its focus on innovation, quality, and rapid response to clinical needs. Its portfolio includes advanced technologies supporting critical care, emergency response, and life sustaining therapies, used by healthcare providers worldwide. The organization combines deep technical expertise with a mission driven culture, investing heavily in research and development to deliver dependable solutions where performance and reliability are paramount. Employees work in a collaborative, engineering driven environment that values hands on problem solving, accountability, and continuous improvement-playing a direct role in creating technologies that help save lives. Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay range for this position is $35.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irvine,CA. Application Deadline This position is anticipated to close on Jul 1, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: . click apply for full job details

Job Description Job Description Job Title: Engineering - Non Degreed I Job Description This position is responsible for the production of high-quality medical device instruments, involving detailed assembly and testing of various electronic components and finished devices within a controlled manufacturing environment. Responsibilities Perform testing of electronic components and assemblies using automated test equipment. Conduct mechanical assembly of electromechanical subassemblies and devices. Read, comprehend, and follow written procedures, as well as understand and follow verbal instructions. Instruct others in the use of all manuals, test procedures, and documentation associated with specialized equipment. Read and interpret engineering drawings, schematics, and complex test procedures. Participate in continuous improvement and quality initiatives to enhance production processes and achieve quality and profitability metrics. Maintain accurate records to ensure Device History Records and quality documents are precise, ensuring all parts are traceable and quality issues can be addressed. Prioritize work by determining the sequencing and timing of different jobs based on precedence and importance. Represent the company positively during tours by demonstrating techniques and sharing appropriate information. Support all company initiatives as identified by management, including Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Comply with U.S. Food and Drug Administration (FDA) regulations and other regulatory requirements, company policies, operating procedures, processes, and task assignments. Adhere to all environmental health and safety SOPs, equipment policies, and procedures, including any department-specific requirements. Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Essential Skills Experience with electronic assembly and testing in the medical device industry is preferred. High School Diploma or equivalency is required; AAS is preferred. 2 or more years of experience with electromechanical assemblies or electronic manufacturing is preferred. Additional Skills & Qualifications Experience in troubleshooting equipment, building, and testing electronic assemblies. Working knowledge of IPC standards and use of complex tools and equipment specific to functional areas. Experience in GMP and FDA-controlled environments is preferred. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Strong verbal and written communication skills with the ability to effectively communicate at multiple levels in the organization. Ability to multitask, prioritize, and meet deadlines in a timely manner. Strong organizational and follow-up skills, as well as attention to detail. Ability to maintain regular and predictable attendance. Ability to work scheduled overtime as required is preferred. Ability to handle and lift up to 25 lbs. as needed for specific job functions. Must be able to sit and/or stand for long periods of time. Ability to frequently sit, stand, walk, reach within hands and arms length, stoop, kneel, and crouch. Work Environment This is an hourly test technician role, conducted 100% onsite. The position operates on the 1st shift with details (5/8) Mon - Fri from 6 am to 2:30 pm. The training schedule includes Monday from 8:45 am to 3:30 pm, Tuesday from 7:00 am to 3:30 pm, and 6:00 am to 2:30 pm for the next eight days. The work environment involves a controlled manufacturing setting with a focus on safety and regulatory compliance. Job Type & Location This is a Contract position based out of Irving, TX. Pay and Benefits The pay range for this position is $20.00 - $20.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irving,TX. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Description Job Title: Electrical Project Manager Job Description The Electrical Project manager/engineer provides technical expertise for mechanical systems in a paint production environment by designing, managing, and implementing equipment solutions that support the department's business plan and long-term sustainability. This role focuses on improving equipment performance, introducing new technologies, and ensuring robust technical documentation and training to enhance safety, quality, cost, delivery, morale, and environmental performance. Responsibilities Develop, manage, and implement established evaluation flows (E-Flow) for investment projects to ensure alignment with business plan targets. Complete equipment improvement activities and lead the decision-making process to enhance equipment characteristics that enable associates to perform successfully. Adhere to equipment installation standards, including drawings, compliance requirements, and data collection, to improve mean time between failures (MTBF) and mean time to repair (MTTR). Drive, support, and develop engineering solutions to solve complex equipment and process problems in order to achieve departmental performance targets. Support the introduction of new technologies into the paint department and provide related technical training to drive continuous process improvement. Use data analysis and customer feedback to identify potential equipment and process problems and implement effective countermeasures to reduce impact on safety, quality, cost, delivery, morale, and environmental metrics (SQCDME). Develop and maintain technical documentation and procedures to ensure equipment and processes meet design intent and support long-term production sustainability. Develop the capabilities of yourself, colleagues, and team members through training, mentoring, and sharing of technical experiences to strengthen the team's skill set. Share engineering technical knowledge and changes clearly through verbal and written communication with internal and external customers to strengthen departmental and plant performance. Identify gaps related to equipment performance and reliability, and develop, lead, and actively participate in improvement activities focused on SQCDME objectives. Essential Skills 2-6 years of engineering experience, preferably in equipment or mechanical engineering roles. Experience in equipment engineering with a focus on mechanical systems and equipment troubleshooting. Strong mechanical engineering knowledge, including equipment installation and layout design. Proficiency in project management, including project scheduling and coordination with stakeholders. Experience with Catia 3D Design or equivalent 3D design software. Proficiency with Microsoft Office Suite, including Excel, Word, and PowerPoint. Ability to perform root cause analysis and apply problem-solving methodologies. Ability to create clear and effective technical presentations. Strong communication and presentation skills, both verbal and written. Ability to teach and train others on technical topics and new technologies. Additional Skills & Qualifications Bachelor's degree in Mechanical Engineering, Electrical Engineering, Applied Manufacturing Engineering, or equivalent work experience. Experience in equipment engineering within a manufacturing or paint production environment. Familiarity with FMEA (Failure Modes and Effects Analysis) and other risk assessment tools. Experience in vendor management and coordination for equipment procurement and installation. Experience in design and troubleshooting of mechanical systems and equipment. Ability to develop and maintain technical documentation and standard procedures. Strong organizational and time-management skills to handle multiple projects and priorities. Work Environment This role operates within the Paint L1 department in a production environment that focuses on paint processes and mechanical equipment. The Equipment Engineer works closely with cross-functional teams, including production, maintenance, and engineering, and regularly interacts with internal and external stakeholders. The environment involves working around industrial equipment and systems, using 3D design software such as Catia and standard office tools including Microsoft Office. The position typically follows standard working hours, with potential need to be on-site during equipment installations, improvements, or troubleshooting activities. The role requires adherence to all plant safety procedures and operational standards appropriate for a paint and manufacturing facility Job Type & Location This is a Contract position based out of Birmingham, AL. Pay and Benefits The pay range for this position is $40.00 - $48.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Birmingham,AL. Application Deadline This position is anticipated to close on Jul 3, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.