Joule

Job Title: Laboratory Technician Location: Flanders, New Jersey Type: Contract Contractor Work Model: Onsite Hours: Monday-Friday Responsibilities: Evaluate liquid product properties using established test methods Perform application testing Generate samples as needed from product formulations Record observations and test results clearly and accurately Independently execute work assignments Maintain laboratory equipment and supplies Adhere to all laboratory safety rules and guidelines Clean and maintain the laboratory and equipment to support a safe working environment Requirements: AS or BS in Chemistry or related field 0-3 years' experience in a laboratory setting Proficient in Microsoft Word, Excel, and PowerPoint Basic knowledge of coatings, test methods, or application techniques is a plus Results-driven Exhibits and fosters team behavior Ability to understand written instructions, test procedures, and Safety Data Sheets (SDS) Good communication, presentation, and organizational skills Ability to think creatively System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Job Title: Assistant Scientist Location: Seattle, WA Hours/Schedule: Monday-Friday 9am-5pm Compensation: $33.59 - $42.67/hr Type: Contract Responsibilities • Design and execute experiments in the process development labs which includes aseptic processing and operation of automated process equipment. • Summarize experimental data and aid in analysis to draw conclusions. • Coordinate with the analytical group for timely delivery of process samples and turn-around of analytical data. • Support production related investigations, ensuring compliance with internal standards and regulatory requirements. • Develop and execute manufacturing process changes and improvement activities, and/or author technical reports for process changes and improvements. • Support process comparability and process validation studies including planning, execution, and documentation management. Support necessary technical experiments and analysis to enable decisions related to raw materials changes. • Flexibility with work schedule as maintenance of cell cultures on occasional weekends, early mornings, or evenings is required Requirements • Degree in Biological Sciences, Chemical Engineering, Life Sciences or related discipline. • BS degree with minimum of 2+ years of relevant experience, or MS degree with minimum 0+ years of relevant experience in biologic process/analytical development or commercial biologic manufacturing process support. • Excellent documentation skills and attention to detail with cGMP experience a plus. • Ability to effectively work in cross functional teams, meet deadlines, and prioritize responsibilities. • Experience working in a self-driven, performance/results oriented, fast paced matrix environment. • Excellent problem-solving skills. • Able to creatively manage time and elevate relevant issues to project lead and line management. • Strong scientific and technical writing with excellent oral communication skills. Preferred Qualifications: • Experience with cell therapy process development or manufacturing • Proficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab) • Experience executing investigations in support of commercial manufacturing • Experience with commercial product support, i.e. post-marketing commitments, on-going validation and comparability • Combination of experience in process development, MSAT and quality. • Operational excellence training/background Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref:

Job Title: Microbiology Technician Location: Elizabeth, New Jersey Type: Contract-to-Hire Work Model: Onsite Hours: 6:00 AM - 2:30 PM (flexible; rotating schedule) Compensation: $23/hour Position Overview We are seeking a Microbiology Technician to join our team. This is a temp-to-hire role, with opportunities for recent BS graduates in Microbiology. Candidates who have graduated from lab certificate programs also encouraged to apply. The technician will support lab operations in a fast-paced, GMP/GLP-compliant environment. Key Responsibilities Perform microbiology testing and lab procedures. Maintain accurate documentation of experiments and results. Follow safety protocols, GMPs, GLPs, and sanitation procedures. Read and interpret safety rules, operating instructions, and procedure manuals. Prepare routine reports and communicate effectively with team members, vendors, and management. Perform basic mathematical calculations, including addition, subtraction, multiplication, division, percentages, ratios, and bar graph interpretation. Maintain consistent attendance and flexibility with rotating schedules. Schedule Example Sunday: 6:00 AM - 11:00 AM (unless additional testing is required) Monday: 6:00 AM - 2:30 PM Tuesday: OFF Wednesday: 6:00 AM - 2:30 PM Thursday: 6:00 AM - 2:30 PM Friday: 6:00 AM - 2:30 PM Saturday: 6:00 AM - 11:00 AM (unless additional testing is required) Notes: Each day, 1-2 people may have late shifts to complete remaining work. On rare occasions, arrival may be required at 4:30 AM - 5:00 AM. Work every holiday; employee day off changes weekly. Attendance and schedule flexibility are essential. Qualifications / Must Haves Associate degree (AA) or equivalent combination of education, training, and/or experience. BS in Microbiology acceptable for recent graduates. Lab certificate programs acceptable. Microbiology experience from academic or lab settings. Knowledge of GMPs, GLPs, and sanitation procedures is a plus. Strong communication skills, both written and verbal. Ability to perform basic math and interpret data graphs. Ability to work in a fast-paced environment with rotating schedules. Driver's license required. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref:

QC Analyst Requirements: -Min. BS/BA Biology, Chemistry, or Medical Technology - 3-6 months of research experience (could be academic, internship, co-op) or industry experience Roles and responsibilities: Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product Interprets test results against specifications and decides if assays pass or fail Maintains documentation of all work performed in accordance with GMP requirements Performs product stability, proficiency, environmental testing and water system testing Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of lab equipment Updates departmental SOP's and QC Monographs as directed Performs microbial testing per SOP's and QC Monographs As well as below: Orders required laboratory supplies, reagents and other consumables Monitors proper storage conditions and expiration dates Disposal of hazardous and bio-hazardous materials Maintains retain samples in accordance with established procedures Maintains statistical process control charts and other tracking reports Ref:

Job Title: Mass Spectrometry Scientist - REACH Scientist Location: Naugatuck, Connecticut Hours/Schedule: M-F, 8 AM - 5 PM Type: Contract Overview Our client, a global chemical manufacturer, is seeking a Mass Spectrometry Scientist - REACH Scientist to support their regulatory compliance and analytical chemistry initiatives. This role offers the opportunity to leverage mass spectrometry expertise to drive key projects, including compliance with European REACH regulations, and contribute to the analysis and interpretation of complex mixtures. The ideal candidate will possess deep experience in various types of mass spectrometry and demonstrate strong problem-solving and communication skills. Responsibilities Perform routine and specialized mass spectrometry analyses as directed by the Mass Spectrometry Lead. Conduct experiments to support REACH (Registration, Evaluation, Authorization, and Restriction of Chemicals) regulatory compliance for products marketed in the European Union. Analyze data, draw scientific conclusions, and communicate results clearly in both verbal and formal written reports to internal stakeholders. Collaborate with scientists to compile data and prepare reports. Develop and optimize separation techniques, ionization methods, and analysis parameters for complex mixtures. Participate in company programs such as safety initiatives, performance culture efforts, and administrative activities including HR processes. Requirements Ph.D. in Chemistry, Biochemistry, or related field with 5+ years of relevant industry experience; or BS/MS with 10+ years of experience. Advanced proficiency with mass spectrometry techniques, including GC-MS, GC-MS/MS, and LC-MS/MS. Strong verbal and written communication skills, including the ability to deliver scientific presentations. Basic understanding of lubricant chemistry is a plus. Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref:

Job Title: Maintenance Technician Location: Greater Lakewood CO area - On-site Hours/Schedule: Multiple shifts available (see below) Compensation: $30 - $38/hour + shift differentials, overtime eligibility, and bonus Type: Direct Hire Shift Options 2nd Shift: Sunday - Tuesday, rotating every other Wednesday (5:30 PM - 6:00 AM) 4th Shift: Thursday - Saturday, rotating every other Wednesday (5:30 PM - 6:00 AM) Overview A global leader in medical technology is seeking experienced Maintenance Technicians to support operations at their newly built, state-of-the-art facility in Littleton, CO. If you want to contribute to the production of life-saving devices while growing your technical career, this is your opportunity! Responsibilities Perform preventive and corrective maintenance on manual, semi-automated, and fully automated equipment Troubleshoot and repair mechanical, pneumatic, hydraulic, control, and electrical systems Participate in equipment performance improvement initiatives and process validation Diagnose and resolve equipment issues independently, with a focus on quality and reliability Implement permanent corrective actions to reduce repeat failures Requirements 2-5 years of experience with troubleshooting mechanical, electrical, pneumatic, and hydraulic systems 2+ years of hands-on PLC experience required Experience supporting manufacturing in regulated environments (medical device, pharmaceutical, biotech, defense, or aerospace) Familiarity with PLCs, Ethernet communication, DeviceNet, and industrial networks Experience conducting root cause analysis Must be up to date on all required vaccinations Must be legally authorized to work in the United States for any employer High School Diploma or GED required System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref:

Job Title: Associate Director, Safety Statistician Location: REMOTE - Must be based in EST or CST time zones only (with occasional travel to NJ) Type: Direct Hire with sponsor client Target Base Compensation: $180k-190k salary (dependent on experience; might have flex for higher salary if exceeding requirements) Annual bonus, RSUs, 401k match, PTO/Personal/Sick time and a comprehensive health benefits package. Minimum Requirements: PhD in Statistics or Biostatistics 2+ years Oncology Safety Signal experience as a Statistician Recent Oncology experience Phase II-III Prior leadership experience Job Summary: Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical aspects for safety signal detection and characterization for ongoing studies and compound-level pooled clinical trial data of project(s). Act as a statistical expert consultant within the company for safety analyses. Responsibilities: Lead for safety signal statistical handling, lead the statistical support in safety signal detection, validation, characterization, and reporting in collaboration with the safety programming team, CSPV, and epidemiology for several projects with minimal direction from the group head, and provide statistical scientific leadership for clinical trial safety data. Lead the statistical support for safety signal monitoring for ongoing trials. Safety analysis methodology and standardization, develop and support statistical safety analysis methodology and standardization across the clinical development in cross-functional teams. Builds partnerships with safety programming teams, project statistical teams, and internal cross-functional teams and external institutions to maximize available resources. Safety working groups and initiatives represent statistics to participate (and lead if applicable) in safety signal working groups or cross-functional initiatives. Education: PhD In statistics or Biostatistics required Experience: Minimum 5 years of relevant experience in the pharmaceutical industry and experience as a safety statistician required. Travel: 10% System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref:

Job Title: Downstream Associate Scientist Location: Seattle, WA Hours/Schedule: M-F; Standard Business Hours Compensation: $46.38 - $58.90/hr Type: Contract Responsibilities Design, execute, and troubleshoot downstream development experiments supporting next-generation lentiviral vector production Identify, onboard, and develop novel downstream technologies in collaboration with internal and external partners Provide experimental design and executional support to team members Support cross-functional development efforts e.g. downstream process development, high-throughput process development Perform hands-on experimental work in the early-phase development and optimization of primarily downstream (clarification, chromatography, tangential and normal flow filtration) unit operations for viral vector production Work independently and within teams to design, execute, and analyze experiments Maintain accurate and detailed laboratory notebook and documentation Summarize and present data in group meetings and contribute to group discussions and team strategy Author technical reports and study memos Requirements B.S. with 2+ years of experience or M.S. with 0-2 years of hands-on downstream experience Experience with Akta Avant chromatography systems and Unicorn software Experience with automated and semi-automated filtration systems (Pendotech, Repligen KR2i, Ambr Crossflow, etc) Hands-on process development experience Independently motivated with ability to multi-task, problem-solve, and coordinate activities within a team Ability to design experiments with design of experiment (DOE) approaches, perform experiments, and interpret the results using statistical software (ex. JMP) Preferred Qualifications: Degree in biological or chemical engineering, biochemistry, or bio-related field Experience in the development of viral vectors (e.g. adeno-, retro-, lenti-), including successful transfer for GMP manufacturing Experience with single-use technologies Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref:

Title: Food Scientist Location: Quincy MA Schedule: M-F 8-5 onsite daily Start ASAP Education: BS/MS/PhD in Food Science/Engineering/related science or engineering field Requirements: 4+ years of experience in Beverage Product Development. Knowledgeable about food chemistry, sensory, microbiology, food packaging systems and food engineering. Ability to work with cross-functional teams at multi levels within the organization Able to work independently, problem solve Oversee a team of 2 scientists and 2 lab tech as needed Responsibilities: Conduct research including new product research and the development of foods. Develop new and improved methods and systems for food processing, production, quality control and packaging. Work in pilot plant and support production scale ups and commercialization's. Field customer requests both internal and external to satisfy project needs from a conceptual phase through commercialization and troubleshooting. Participate in ideation/brainstorming Develop gold standards while working with Culinary and subject matter experts (SMEs) Match competitive products Formulation Optimization Concept to Commercialization Execute internal processes Ability to understand and troubleshoot customer processes Be a strong part of customer facing team to deliver solutions that will "Nourish and Delight" our customers. Coordinate customer calls with sales/culinary representatives through presentations both technical and culinary based. Work with cross functional groups to optimize the strengths of the various teams and deliver the best Taste and Nutrition experience for our customers Develop and protect Intellectual Property by documenting research notes. Study methods to improve quality of foods such as flavor, color, texture, nutritional value, convenience, or physical, chemical, and microbiological composition of foods Complete project requests within the time frame required by the customer. Assist customers with technical issues that may arise. Travel to Kerry production plants and to customers. Must be able to taste and smell chemicals, flavors and food products. Must be able to stand for long periods of time in a laboratory setting and lift 50 pounds. Ref:

Job Title: Assistant/Associate Scientist Location: Seattle, WA Compensation: $40.00- $50.30/hr Type: Contract, Potential for extension or conversion to permanent Responsibilities Oversee lab activities and schedule Design studies to support commercial manufacturing deviation investigations. Support the the execution of process characterization studies. Collaborate with commercial vector team to identify opportunities for process improvements, make formal recommendations. Lead identification and implementation of new technologies and procedures from Development into Manufacturing Lead efforts focusing on alignment and harmonization of manufacturing process across multiple sites Support the hands-on training of commercial process unit operations to Vector MS&T Identify, design and manage small capital engineering projects Requirements Degree in Biology, Chemistry, Biochemical or Chemical Engineering, or equivalent area of related experience in biologics upstream manufacturing Preference given to candidates with experience performing process characterization Knowledge of cellular immunology and/or vector manufacturing a plus Experience with cGMP, ICH guidelines, PPQ (process validation), control strategy development, and working within a Quality organization Proficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab) Experience working in a self-driven, performance/results oriented, fast paced matrix environment Experience writing experimental plans and protocols Physical Demands: Position requires repetitive use of hands and wrist (computer work), and infrequent lifting of items not to exceed 50 lbs Occasional bending, twisting and stooping to allow for gowning into classified environment required Work Environment: Position will require time in the office and lab Position is a team & project-based position that will require occasional shift work, weekends, and holidays Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref:

Title: QA Associate Location: Devens, MA Start date: ASAP Responsibilities: Provide Quality assistance and oversight to operations, for in-process intermediates and manufactured products, and other GMP processes as required. Performs review and approval of documentation associated with in-process materials, and manufactured product. Assists in the identification, generation and quality review of investigation records that may result during day-to-day operations. Assure the quality of manufactured products complies with all applicable regulations and guidelines. Performs routine manufacturing batch production record review in support of product release in accordance with specifications and SOPs. Perform walkthroughs of GMP areas documenting observations and areas of concern to support inspection readiness of the manufacturing facility and support areas. Supports return to service walkthroughs and Manufacturing inspection readiness walkthroughs per procedures as needed. Assures all electronic and paper documentation, which requires QA review is in compliance with corporate and site procedures, cGMP regulations, and other industry guidelines. Reviews, approves and provides guidance for quality master data Authors and revises Quality specific SOPs and may provide Quality review and approval of manufacturing related SOPs. Monitors and trends batch record errors, batch record review cycle time to support disposition, and walkthrough observations to provide Quality Assurance management with quality indicator data. Assist Operations by providing quality oversight and guidance for atypical events. May provide guidance to less experienced staff. May support the Quality approval of Master Batch Records. Supports the Quality review and closure manufacturing deviations. May support release of incoming or manufactured products. Other duties as assigned. Requirements: Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent is preferred. A minimum of 4 years of relevant experience in a regulated environment with 2 years focused on product quality preferred Knowledge of biotech bulk and finished product manufacturing, analytical testing is highly desirable. Knowledge of US and EU cGMP regulations and guidance. Knowledge of electronic batch record systems, DeltaV, and other electronic systems applicable to laboratory test result generation, inventory management, investigations and equipment tracking and maintenance is desirable. Joule, a System One division is a leader in specialized workforce solutions and integrated services. With more than 6,000 employees and roughly 50 offices throughout the U.S. we provide scientific, clinical, engineering, energy, IT, legal and administrative staffing services. For more than 40 years, we have delivered workforce solutions and integrated services to clients nationally.

Title: Laboratory Chemist Location: Poughkeepsie, NY area Duration: Contract to hire Schedule: M-F Full Time Target Start Date: ASAP Responsibilities: Performing routine chemical tests and assays on pharmaceutical raw materials and finished products. Analyze pharmaceutical finished dosage forms by HPLC. Prepare test solutions and reagents and maintain chemical inventory. Assist in training new laboratory personnel. Ensure all necessary information is recorded in a laboratory notebook. Assure that all testing and documentation comply with cGMP's. Write SOP's as required. Perform minor maintenance and repairs on instruments and equipment. Requirements: BS Chemistry or related Science Recent grads up to 3 years experience (academic research/ internship/ co-op or in pharma industry) Knowledge of IR, HPLC, and wet chemistry (Pipetting, titration, measuring PH, moisture analysis, dissolution) Familiarity with cGMP's and GLP's a plus Joule, a System One division is a leader in specialized workforce solutions and integrated services. With more than 6,000 employees and roughly 50 offices throughout the U.S. we provide scientific, clinical, engineering, energy, IT, legal and administrative staffing services. For more than 40 years, we have delivered workforce solutions and integrated services to clients nationally.