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The Amazon Regulatory Intelligence, Safety, and Compliance (RISC) team is seeking an exceptional Applied Scientist to tackle complex compliance challenges. In this high-impact role, you will leverage your deep technical expertise and customer-obsessed mindset to design and evaluate state-of-the-art algorithms in risk modeling, computer vision, and natural language processing. You will translate complex business requirements into well-defined science problems and work collaboratively with product, engineering, and business stakeholders to drive real-world impact. Staying at the forefront of applied machine learning, you will continuously adapt your skills to tackle new challenges. Contributing to Amazon's scientific thought leadership, you will author high-quality research papers for internal and external conferences. This is an opportunity to apply your technical skills in a fast-paced, highly collaborative environment, making a meaningful difference in the lives of Amazon's customers. If you have a passion for solving complex problems and a customer-centric approach, we encourage you to apply for this exciting role. Key job responsibilities - Explore the use of reinforcement learning, multi-agent systems, and meta-learning to build autonomous AI agents that can adapt to new challenges and support complex decision-making. - Design and evaluate state-of-the-art algorithms and approaches in risk modeling, using techniques such as graph neural networks, deep learning, and boosted trees to detect anomalies, fraud, and policy violations. - Develop advanced multi-modal and large language models to classify product content, understand customer intent, and retrieve relevant information. - Collaborate closely with product managers, engineers, and business stakeholders to validate hypotheses, drive adoption, and maximize the real-world impact of your work. - Translate complex product and customer experience requirements into well-defined, measurable science problems and KPIs, contributing to Amazon's scientific thought leadership through high-quality research papers. A day in the life - Understanding customer problems, project timelines, and team/project mechanisms - Proposing science formulations and brainstorming ideas with team to solve business problems - Writing code, and running experiments with re-usable science libraries - Reviewing labels and audit results with investigators and operations associates - Sharing science results with science, product and tech partners and customers - Contributing to team retrospectives for continuous improvements - Participating in science research collaborations and attending study groups with scientists across Amazon BASIC QUALIFICATIONS - PhD, or Master's degree and 5+ years of applied research experience - Experience programming in Java, C++, Python or related language - Experience with neural deep learning methods and machine learning PREFERRED QUALIFICATIONS - 7+ years of building machine learning models for business application experience Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $150,400/year in our lowest geographic market up to $260,000/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit . This position will remain posted until filled. Applicants should apply via our internal or external career site.

About Us Pace Life Sciences Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations. Job Description Scientist II SUMMARY Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions. ESSENTIAL FUNCTIONS Serves as a lead to staff to include providing work direction, guidance, and training. Overseeing or reviewing, completing, and processing comprehensive types of forms, documents, databases, and related materials and information. Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Provides training and guidance on analytical tests, methods, and instrumentation, as required. Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients. Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, among others. Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards. Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONS Education and Experience Bachelor's degree in chemistry/biochemistry, or a closely related field. Three to five (3-5) years of experience, including experience with specialized or technical programs or operations; OR an equivalent combination of education, training, and experience. Master's or PhD degree is strongly preferred. Required Knowledge and Skills Required Knowledge Complex to specialized principles, practices, and techniques of chemistry/biochemistry and formulation development. Broad understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures. Complex to specialized methods to resolve chemistry/biochemistry problems, questions, and concerns. Broad understanding of applicable chemistry/biochemistry laws, codes, and regulations. Understanding of broad testing tools, equipment, and calibration. Computer applications and systems related to the work. Principles and practices to serving as an effective project team member. Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. Correct business English, including spelling, grammar, and punctuation. Required Skills Performing complex to specialized professional-level chemistry/biochemistry duties in a variety of assigned areas. Overseeing and administering broad and varied chemistry/biochemistry/formulation functions. Ability to operate and train others in analytical instruments and manufacturing equipment. Training others in policies and procedures related to the work. Serving as a team member and the development and management of projects. Operating in a both a team and individual contributor environment. Interpreting, applying, and explaining applicable laws, codes, and regulations. Preparing advanced to expert functionals reports, correspondence, and other written materials. Using initiative and independent judgment within established department guidelines. Using tact, discretion, and prudence in working with those contacted during the work. Performing effective oral presentations to large and small groups across functional peers and the department. Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. Establishing and maintaining effective working relationships with various individuals contacted in the work. Additional Information Benefits 80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Pay Range/Compensation $70,000 per year Work Schedule Monday through Friday, 8:30 AM to 5:00 PM

About Us Pace Life Sciences Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations. Job Description Scientist I SUMMARY Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions. ESSENTIAL FUNCTIONS Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Provides training and guidance on analytical tests, methods, and instrumentation, as required. Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients. Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, among others. Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards. Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONS Education and Experience Bachelor's degree in chemistry/biochemistry, or a closely related field. 5-7 years of experience, including experience with specialized or technical programs or operations; OR an equivalent combination of education, training, and experience. Required Knowledge and Skills Empower Master Control LIMS UV -Vis Dissolution HPLC GMP ALCOA+ Root Cause Analysis Additional Information Benefits 80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Work Schedule Monday through Friday, 8:00 AM - 4:30 PM

About Us Pace Life Sciences Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations. Job Description Scientist I SUMMARY Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions. ESSENTIAL FUNCTIONS Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Provides training and guidance on analytical tests, methods, and instrumentation, as required. Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients. Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, among others. Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards. Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONS Education and Experience Bachelor's degree in chemistry/biochemistry, or a closely related field. Two to three (2-3) years of experience, including experience with specialized or technical programs or operations; OR an equivalent combination of education, training, and experience. Required Knowledge and Skills Required Knowledge Complex to specialized principles, practices, and techniques of chemistry/biochemistry and formulation development Broad understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures. Complex to specialized methods to resolve chemistry/biochemistry problems, questions, and concerns. Broad understanding of applicable chemistry/biochemistry laws, codes, and regulations. Understanding of broad testing tools, equipment, and calibration. Computer applications and systems related to the work. Principles and practices to serving as an effective project team member. Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. Correct business English, including spelling, grammar, and punctuation. Required Skills Performing complex to specialized professional-level chemistry/biochemistry duties in a variety of assigned areas. Overseeing and administering broad and varied chemistry/biochemistry/formulation functions. Ability to operate and train others in analytical instruments and manufacturing equipment. Training others in policies and procedures related to the work. Serving as a team member and the development and management of projects. Operating in a both a team and individual contributor environment. Interpreting, applying, and explaining applicable laws, codes, and regulations. Preparing very complex to specialized functionals reports, correspondence, and other written materials. Using initiative and independent judgment within established department guidelines. Using tact, discretion, and prudence in working with those contacted during the work. Performing effective oral presentations to large and small groups across functional peers and the department. Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work. Additional Information Benefits 80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Work Schedule Monday through Friday, 8:00 AM - 4:30 PM

MS&T Scientist III As the MS&T Scientist III, the successful candidate will work on significant technical/scientific project activities to execute strategies and technical solutions that meet companys and their clients needs and expectations through broad expertise. The successful candidate will be expected to maintain a high level of expertise within their field and engages in creation of processes and equipment design for clinical, scale up, and/or registration batches, including technology transfer of projects from client sites. Assume technical ownership of a given product across the various stages of development and commercialization in coordination with other functional areas. The MS&T Scientist III will be responsible for designing, leading, and executing studies to support product and process optimization and automation, investigation on deviation and root cause analysis; technology transfer activities, and product characterization studies, and any other activities required by the MS&T organization. RESPONSIBILITIES * Utilize and apply knowledge of basic scientific principles, theories and concepts to develop solutions to problems of moderate to high complexity.Lead multidisciplinary teams in developing and implementing solutions. * Perform site transfer activities to company from business partner locations and provide scientifically sound development reports. * Develop and optimize manufacturing processes for clinical, registration and commercial scale batches for sterile and non-sterile formulations. * Prepare and review Master Batch Records for experimental/engineering, registration, scale-up and process validation batches. * Prepare robust pharmaceutical/process development reports and other CMC documentation for regulatory submissions and represent company as SME during internal/external regulatory audits. * Use statistical process control and other statistical tools for comparison and hypothesis testing. Apply engineering, pharmaceutical sciences or materials sciences fundamentals to model the product and process to solve complex technical problems. * Evaluate and implement advance technologies for process evaluations and optimization (e.g., Process Analytical Technology, electronic batch records etc.) * Review and provide inputs for validation master plans, validation protocols, validation reports, continued process verification (CPV) plans and statistical sampling plans, among other important strategic documents. * Acts as internal/external Subject Matter Expert (SME) for drug product and process related technical issues and provide technical support to Formulation, Manufacturing, and Quality. * Identify potential root causes of variation and deviations using a systematic approach. Expertise in use / application of variety of problem-solving tools e.g. Ishikawa, Kepner-Tregoe (KT), five-whys, etc. and lead technical Deviation write-ups and CAPA assignments. * Work closely with process engineering team to develop robust user requirement documents for process equipment including manufacturing and packaging. * Provide technical input to management team regarding site capacity to evaluate new projects. * Lead and guide other scientists/associates in process development and manufacturing. QUALIFICATIONS * Experience in cGMP manufacture of commercial or late phase clinical products. * Experience with technology transfer and scale up * Familiarity with statistical process control (SPC), complex data analysis, mathematical modeling, and optimization software (like MiniTab, JMP, etc.) is a must. * Knowledge and experience in cGMP, risk assessment and investigation tools and techniques. * Able to work on multiple projects simultaneously. Familiarity with project management concepts is preferred. * Proficiency with Quality by Design (QbD) concepts and design of experiments required. * Demonstrated ability to provide scientific input and make decisions to resolve problems with minimal supervision. * BS/MS/PhD in pharmaceutical sciences/chemistry (or related field like organic, physical, biochemical, chemical engineering) with 6+ years (BS,), 4+ years (MS) or 2+ years (Ph.D.) industrial GMP experience.

Scientist II - Quality Assurance Specialist role, non laboratory role working in an office setting (desk role) reviewing and supporting Scientists work from the Analytical Chemistry department. Pace Analytical Life Sciences (PLS) in Norristown, PA is an industry leading contract lab supplying, formulation development, clinical trial manufacturing and analytical chemistry services to the Pharmaceutical, and Life Sciences industry. This position would be at Pace Analytical Life Sciences in Norristown, PA. This is a full-time, day shift, permanent position. Summary: Employees are exposed to a varied and challenging range of product development projects in a dynamic, fast-paced, rewarding, work environment, with state of the art equipment. Primary Responsibilities: Review and approve analytical documentation in accordance with company policies and current Good Manufacturing Practices (cGMP's) Review documentation to support the analytical chemistry department in accordance with company policies and current Good Manufacturing Practices (cGMP's) including but not limited to: dissolution, HPLC and other analytical chemistry techniques Review laboratory or quality control data pertinent to approved analytical monographs, validation protocols and/or applicable USP test methods Prepare, review, approve and implement Standard Operating Procedures (SOP's) Initiate proper change control, deviation, out of specification and investigation documentation when required Update pertinent logs and tracking systems as they relate to the company's Manufacturing and Quality Systems Report any critical issues to appropriate management in a timely manner To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Education and Experience: Bachelor's degree in chemistry or a closely related field; AND 5 years of chemistry experience, including experience with complex programs or operations; OR an equivalent combination of education, training and experience. Required Knowledge and Skills Minimum of 5 years' experience working as an Analytical Chemist/Scientist in a pharmaceutical environment; prior QA or Peer Review experience strongly preferred Previous experience with solid dosage formulations including a thorough understanding of analytical testing and validation methodologies is required HPLC experience required Previous experience working with Phase I and Phase II development preferred Proficient in Microsoft Word and Excel and/or other office or computer applications as required Must be a motivated, well-organized individual with the proven ability to multi task Possess strong attention to detail and can effectively communicate information to appropriate parties through verbal and written communication Ability to work individually or as a team while possessing strong interpersonal skills Have knowledge of various regulatory systems and guidelines (SOP's, cGMP's, IPEC, etc.) Have the desire to work in a small entrepreneurial environment Other duties as assigned. Physical/Mental Requirements: The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone. Working Environment: Work is performed in a lab and office setting. Work is subject chemicals, fumes, gasses, noxious odors and related items in a lab setting. OFCCP Statement Pace Analytical is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity. First shift Monday through Friday role. From time to time the need to come in early, stay late, and occasional weekend work.

Overview: Avomeen, proud to be a part of Element has an opportunity for a Chemist to join our rapidly growing Life Sciences group.The Chemist will test, develop and improve formulations in consumer products opportunity space, perform testing using a variety of technologies and draw conclusions based upon analytical data. Work is performed under the supervision of the lab manager. Element's Life Sciences group supports developers and manufacturers in the antimicrobial, food and nutraceutical, medical device, and pharmaceutical and biotechnology industries. We provide personalized testing solutions and regulatory consulting support to validate the safety and efficacy of our clients' products at every stage of development, production and market release. Responsibilities: Executes projects of moderate complexity in support of client needs. Types of projects include: Product deformulation and product development, method development and validation, failure analysis and problem solving, testing of product or packaging materials for impurities and/or performance, liquid and/or solid dosage formulation, and structural characterization Develops analytical methods and performs testing using a variety of technologies possibly including HPLC, LC-MS, GC, GC/MS, Microscopy, FTIR, UV, EDX, NMR, TGA, DSC and manual lab equipment. Has learned multiple methodologies and techniques to be able to maximally contribute to the organization Follows all safety requirements including wearing appropriate personal protective equipment Generates client reports and supporting laboratory documentation in compliance with company SOPs Complies with all company SOPs and modifies SOPs when directed Takes responsibility for lab instruments and sees to their care and upkeep, engaging external vendors when appropriate Communicates effectively with clients and colleagues through written and oral presentation Is able to develop test methods and technical test protocols Is client focused as demonstrated by delivering projects in a timely manner with minimal errors Able to draw and defend conclusions based upon analytical data Is able to perform Peer Review of the work of others Skills / Qualifications: B.S, M.S. or PhD in Chemistry, Materials Science, Polymer Science or a Related Field 1-3 years' experience or knowledge of analytical chemistry techniques demonstrated through a combination of industry and academic performance Ability to draw and defend conclusions based upon analytical data Ability to function well in a high-paced and at times stressful environment. Proficient with Microsoft Office Suite or related software Good fundamentals and ability to learn quickly #LI-AL1 Company Overview: Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 6,500 brilliant minds operating from 200 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement: At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: race, color, age, religion, gender, national origin, disability, and/or protected veteran status, or other characteristics in accordance with the applicable governing laws. TIC Council Statement: Element is proud to be a full member of the Testing, Inspection & Certification Council (the "TIC Council"), an international association representing independent testing, inspection and certification companies. Members of the TIC Council must implement and abide by the TIC Council Compliance Code. Element has therefore issued an overarching Code of Conduct which is supported by our Compliance Programme. A copy of the Code of Conduct and more information about our Compliance Programme can be found in the section of .

Vaxcyte, Inc. (Nasdaq: PCVX) is a next-generation vaccine company seeking to improve global health by developing superior and novel vaccines designed to prevent some of the most common and deadly infectious diseases worldwide. Our exclusively licensed cell-free protein synthesis platform and our proprietary know how enable us to design and produce optimized protein carriers and antigens, the critical building blocks of vaccines, in ways that we believe conventional vaccine technologies cannot. Our pipeline includes pneumococcal conjugate vaccine, or PCV, candidates that we believe are the most broad- spectrum PCV candidates currently in development, targeting the $7 billion global pneumococcal vaccine market. Our lead vaccine candidate, VAX-24, is a preclinical, 24-valent broad-spectrum pneumococcal conjugate PCV with preclinical proof-of-concept demonstrating potential to replace the standard of care that we expect to advance into clinical trials in the second half of 2021. Our pipeline also includes VAX- XP, a PCV with an expanded breadth of coverage of at least 30 strains, including newly emerging strains responsible for invasive pneumococcal disease and antibiotic resistance; VAX-A1, a prophylactic vaccine candidate designed to prevent Group A Strep infections; and VAX-PG, a therapeutic vaccine candidate designed to slow or stop the progression of periodontal disease by targeting the keystone pathogen responsible for this chronic, oral inflammatory disease. We completed our initial public offering in June 2020, raising $287.5 million in gross proceeds. Summary: Vaxcyte is looking for an energetic and talented individual to join our Formulation and Drug Product Development team. Candidate should be an experienced and flexible individual who would be comfortable working on multiple tasks at once, with excellent communication skills to navigate rapid changes in prioritization. This position is for a scientific role which will be primarily lab based. The candidate will have a good knowledge and practical experience in the field of vaccine formulation. The candidate will also have industry based experience in a range of standard protein biochemistry analytical techniques. Experience in biophysical characterization of formulations would be very beneficial. The primary responsibility for the incumbent will be to support development of projects from the research through the preclinical phase, into early clinical phases and also supporting later stage programs. Essential Functions: • Supporting formulation manufacture for thermal, freeze/thaw, and agitation stability studies on both Drug Substance (DS) and Drug Product (DP) materials • Conducting analysis of these formulations using a broad range of standard protein biochemistry analytical techniques for formulation selection • Supporting formulation comparability studies, container selection and scale up activities • Preparing sterile formulation samples to be used for in vivo testing • Evaluating effect of new formulation components on already established standard analytical assays • Maintaining an accurate and up to date inventory of supplies of DS used by multiple groups Requirements: • BSc or MSc in Pharmaceutics, Chemistry, Biophysics or Biochemistry preferred, or Analytical Chemistry or Biology considered, with >2years of industrial experience • The candidate will have had previous experience in developing formulation of proteins, polysaccharides and/or protein conjugates for adjuvant containing vaccines (other biological experience also considered) • Experience supporting stability studies, including study set up and sample testing and analysis • Experience in using standard protein plate based assays is needed. Some experience in spectrometric methodologies, particle light scattering, quantitative subvisible particle analysis, visible analysis and HPLC/UV is preferred • Experience working under aseptic conditions is necessary • Strong interpersonal skills; ability to communicate effectively both verbally and in written formats (must be able to work with managerial and lab team in remote setting when needed) are necessary to collaborate effectively with the rest of the Formulation and Drug Product Development team • Critical thinking, the ability to analyse data and to report results to the team in a clear and concise manner during group meetings is needed • Eagerness, ability to learn and great flexibility to rapidly switch gears between tasks • Detail oriented, rigorous and excellent skills in record keeping/documentation • Good proficiency in the use of Microsoft office suite (in particular Excel and PowerPoint) Reports to: Senior Scientist in the Formulation and Drug Product Development team Location: Foster City, CA Compensation: The compensation package will be competitive and includes comprehensive benefits and an equity component.

Immediate need for a Job title Formulation Scientist e xperience in the Pharmaceutical Industry . This is6 + Months Contract position for the location Andover, MA . Please review the job description below: Job ID # 21-02421 open to levels I and II The individual in this role will be a highly skilled, meticulous and motivated scientist who will focus on analytical characterization of mRNA and Lipid Nanoparticle (LNP) formulations. He/she will work cross-functionally to design and coordinate analytical characterization characterize and/or implement fit-for-purpose, robust, characterization methods Identify, develop and implement Client biochemical and biophysical methods to further enhance knowledge or to address potential analytical characterization gaps for mRNA and Lipid Nanoparticles He/she will participate in performing biochemical and biophysical characterization (HPLC, cIEF, light scattering, particle characterization, spectroscopy, calorimetry) of lipid nanoparticles, lipids and mRNA. Preparation of samples for characterization studies • Perform analytical testing supporting process development and product release, including spectroscopic, chromatographic, biophysical, and molecular biology techniques Maintain thorough electronic lab notebooks and documentation records Deliver reproducible and impactful results under ambitious timelines • Execute and troubleshoot standard protocols, develop and adapt new protocols into practice, and query literature to incorporate additional assays as needed. Position Comments visible to MSP and Supplier: Intake Notes: Job description has been updated General Analytics Particle Characterization MRNA - experience BS w/0-6yrs MS w/0-2 Our client is a leading Pharmaceutical Organization and we are currently interviewing to fill this and other similar Contract positions. Qualified candidates should apply online for immediate consideration Job Requirements: Responsibilities: open to levels I and II The individual in this role will be a highly skilled, meticulous and motivated scientist who will focus on analytical characterization of mRNA and Lipid Nanoparticle (LNP) formulations. He/she will work cross-functionally to design and coordinate analytical characterization characterize and/or implement fit-for-purpose, robust, characterization methods Identify, develop and implement Client biochemical and biophysical methods to further enhance knowledge or to address potential analytical characterization gaps for mRNA and Lipid Nanoparticles He/she will participate in performing biochemical and biophysical characterization (HPLC, cIEF, light scattering, particle characterization, spectroscopy, calorimetry) of lipid nanoparticles, lipids and mRNA. Preparation of samples for characterization studies • Perform analytical testing supporting process development and product release, including spectroscopic, chromatographic, biophysical, and molecular biology techniques Maintain thorough electronic lab notebooks and documentation records Deliver reproducible and impactful results under ambitious timelines • Execute and troubleshoot standard protocols, develop and adapt new protocols into practice, and query literature to incorporate additional assays as needed. General Analytics Particle Characterization MRNA - experience BS w/0-6yrs MS w/0-2

At Lyell, our vision is to develop curative cell-based immunotherapies for solid tumor cancers. We have innovative science originating from our founder's world class labs and a unique and disruptive approach to research and development. Our company is first and foremost focused on understanding the science. We are a learning organization, dependent on deep collaborative relationships between all of our colleagues, partners and founders. Our culture is based on Science, Respect, Courage and Collaboration and it reflects who we are and the environment we are creating. Lyell Immunopharma is seeking a qualified candidate to join our newly established R&D center in South San Francisco and Seattle as a group leader in the TCR team. The ideal candidate will play a principal role in developing the next generation of cancer immunotherapies. The candidate will be responsible for scientifically supporting the TCR team in developing methods to improve antitumor effects of T cells for adoptive cell therapy. Essential Functions: Design and conducts complex experiments independently with scientific rationale. Can critically analyze experiments and interpret complex data drawing appropriate conclusions. Creative thinking, capable to improve the efficiency of current experiments and assays. Communicate and discuss results with other scientists. If a Scientist, represent Lyell externally through presentations at key National / International meetings, interactions with our key investigators. Participate and thrive in an interactive, team-oriented culture. Preferred Experience: Experience with T cell culture and expansion techniques. Deep molecular knowledge and field expertise in T cell biology with a special emphasis in cellular immunotherapy Proven record of relevant experience and expertise in assays involving measurements related to TCR specificity, tumor killing assays, T cell exhaustion, T cell stemness and T cell functionality. Strong cell/molecular biology knowledge and extensive bench experience. Consistent record of innovative contributions to the T cell biology field and/or cancer immunotherapy as evidenced by first / senior-authored publications in top-tier journals and patent authorship (Optional for scientist). Preferred Education: PhD, MSc or BSc degree in molecular biology, cancer biology, immunology, pathology or related field. Preferred Additional Skills: Experience with general T cell culture work (culture, expansion, media formulations, passaging, preservation, co-culture systems. Tumor co-culture assays. Experience with immunohistochemistry, fluorescent microscopy, RT-PCR and Western and Blotting. Experience with cell cytometry and cell sorting. Experience with transcriptional analysis such as RNA-Seq, ATAC-seq and single cell analysis is a plus. At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees. Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws. We've learned from experience that some of the best people don't always match our requirements perfectly - if you're interested and think you could fit, please don't hesitate to apply.

Regeneron's Formulation Development Group in Tarrytown, NY is seeking an Associate Director to lead their New Technology Group. The Formulation Development Group (FDG) supports multiple modalities & technologies across various stages of development and strives to have an impact across key therapeutic like ophthalmology, infectious diseases, oncology, and immunology. As Associate Director you will lead the research, investigation & development of our novel technologies to address business needs and medical challenges. In this Associate Director role and as lead of the New Technology Group you'll lead, plan and execute activities to support development of drug delivery technologies, formulations, processes and characterization tools. A Typical Day in the Role May Look Like: Lead simultaneous development of several technologies that are applicable to different modalities (e.g. mAbs, fusion proteins, RNA therapeutics), processes (e.g. spray drying, membrane emulsification) and delivery tools (e.g. LNPs, depots, implants, pumps). Will follow strong scientific principles and practices (e.g. QbD) honing in-house tools & prototypes as well as evaluation of external technologies. Act as subject matter authority on sustained/controlled release systems. Will represent (FDG) as a SME in cross-functional settings and Senior Leadership meetings. Lead a team of 5+ scientists, providing scientific & strategic leadership for new technology projects in a cross functional setup. Independently set priorities with FDG's goals & demonstrate strategic and scientific agility (e.g. life cycle management strategies). Ensure strong strategic cohesion & communication with colleagues from Therapeutic Focus Areas, Research groups, Pre-clinical toxicology, Drug Product & Drug Substance Manufacturing, Project Management, Regulatory Sciences, Quality, Business Development, Finance and Marketing. Participate in scientific conferences and forums as Regeneron's new technology representative to gain information about novel products that are pertinent to current and future medical & business needs. Demonstrate scientific excellence through reports, publications and patents. Will be proactive in generating IP and related documentation and effectively collaborate with Regeneron's patent teams. This Role May Be For You If: You possess an in-depth understanding of formulation, process and characterization fundamentals, have strong organization and scientific skills to develop sustained release systems & novel technologies and effectively collaborate within a matrix organization to influence cross-functional teams & senior management You have strong initiative to complete results-oriented tasks and drive new technologies related to Formulation Development. You are capable of multi-tasking, working both independently and within a collaborative environment. This position requires a Ph.D. in Chemical Engineering, Pharmaceutical Chemistry, Pharmaceutical Sciences or Pharmaceutics (or related field) with 8 - 12 years of relevant shown experience. 5 + yrs demonstrated ability in leading a group of scientists. Must have provided mentorship and training to scientists and managers (Ph.D. and M.S. level) and must be a motivating and positive influence on the team. Consistent and proven track record in development of sustained/controlled release systems with experience in technology areas such as cross-linked/modified polymer science, hydrogels, biodegradable polymers, polymer fabrication processes and drug delivery systems. Experience in biologics product development including understanding of formulation, process and characterization fundamentals across modalities (e.g. mAbs, fusion proteins, RNA therapeutics) and delivery forms (e.g. LNPs, depots, implants, pumps) a plus. Experience in developing relationships with external vendors, CROs, academic institutions and scientific leaders. Strong leadership and organization skills with ability to lead cross functional teams preferred. Must be an experienced leader across settings that require frequent interaction with internal and external partners, multi-function departmental leaders as well as senior management. Must have excellent oral and written communication skills. A proven track record to quickly adapt to changes in project direction to meet the constantly evolving demands. Proven ability to think creatively and acquire solutions to complex and diverse problems. Proven record of creative, productive, and insightful analysis and achievement. Proven interpersonal and leadership skills and ability to influence others to achieve results. Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.