Chemist jobs in Brookline, MA - 296 jobs

Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: The Structure Characterization Analytical Scientist will have expertise in structural elucidation of drug substances, impurities and degradants through rapid and efficient characterization of synthetic molecules by NMR, chromatography and mass spectrometry analysis. The successful candidate will have a strong foundation in analytical chemistry and spectroscopy, with hands-on laboratory experience. A background in organic chemistry is highly desirable for interpreting complex structures and reaction mechanisms. Core Responsibilities: Exercise sound technical judgment in the planning, execution, and analysis of experiments to determine structural identification of pharmaceutical actives and related substances including forced degradation for impurity enrichment, 2D NMR, high-resolution MS, HPLC and GC method development. Implement characterization approaches for the preparation, isolation, and identification of low-level impurities in a drug development environment. Author analytical test methods, protocols, reports, relevant SOPs and regulatory documents as needed. Develop and apply qNMR methods for accurate quantification of drug substances and impurities. Support method development, qualification, transfer, and validation activities for analytical procedures. Provide support for cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards. Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies. Collaborate with key partners including chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery. Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing. Maintain and troubleshoot NMR and LCMS instrumentation (e.g., Orbitrap, Q-TOF, Triple Quad). Qualifications: Required Ph.D. or M.S. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or related field. Demonstrated mastery of one or more subject areas related to structural characterization. Strong hands-on experience with 2D NMR, HR-MS. 3+ years of hands-on experience in structural characterization of impurities for active pharmaceutical ingredients under cGMP's. Strong knowledge of organic structure elucidation - forced degradation, MS, NMR, etc., with the ability to train/mentor colleagues. Excellent communication, organizational, and leadership skills with ability to work independently and in a team environment. Well organized with good problem-solving skills, a high level of attention to detail and have a passion for delivering high quality data in a fast-paced environment Preferred Experience with regulatory submissions and GMP/GLP environments. Experience with structural characterization of larger synthetic molecules including peptides and oligonucleotides. Risk assessment and development of trace level methods for potential GTI and nitrosamines. Salary Range : $90,000 - $135,000 annual base salary Our Commitment: Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .

Rangam is seeking candidates for a Direct Hire role as an Associate Scientist, Assay Development with our client, one of the world's largest pharmaceutical companies. Seeking candidates in Cambridge, MA or willing to relocate. Use Your Power for Purpose Client's purpose is to deliver breakthroughs that change patients' lives. At the core of fulfilling this purpose is Research and Development, where we translate advanced science and technologies into the therapies and vaccines that matter the most. You will be at the forefront of this mission, contributing to the discovery and development of innovative treatments that improve patients' lives. Client's BioMedicine Design (BMD) Assay Development group is seeking a highly motivated research associate to establish binding and functional assays and support hit-to-lead discovery of peptide and antibody-based therapeutics. The candidate will play a critical role in the design and execution of biochemical and of cell-based functional assays and high-throughput screening to support the BioMedicine Design portfolio. The candidate will be responsible for the development and execution of experiments using a variety of detection technologies including homogenous technology including HTRF, ELISA/DELFIA, FACS, imaging and cell-based functional assays focused on signaling, proliferation, or cytotoxicity. In addition, the candidate will analyze data, present results at internal meetings, and closely collaborate with project team members to develop strategies and identify lead molecules. We are looking for a creative, solution-oriented individual who enjoys the opportunity to explore new methods. What You Will Achieve In this role, you will: Develop assays to identify and characterize peptide, antibody and multispecific candidates to support programs across multiple therapeutic areas. Biochemical assay formats may include protein binding, competition and enzymatic cleavage assays. Cell based assays may include binding (FACS and ELISA), competition, cell signaling (NanoBiT, calcium flux, cAMP, phospho-protein HTRF/AlphaLISA, etc) and reporter gene assays using a variety of cell lines. Execute high-throughput screens using automated and semi-automated platforms and analyze results. Collaborate with project teams to establish screening strategies, interpret results, and make decisions to drive programs forward. Write protocols, maintain electronic lab notebook, and regularly review literature to maintain knowledge of scientific trends and new technologies. Here Is What You Need (Minimum Requirements): Bachelor's degree and 0-3 years of experience in molecular biology, biochemistry, cell biology or related discipline, along with a basic understanding of biologics drug discovery workflows. Demonstrated experience in assay development and troubleshooting with methods such as HTRF, ELISA/DELFIA, FACS, and cell-based functional assays focused on signaling, proliferation, or cytotoxicity. Demonstrated experience with plate-based assay formats and maintaining cell cultures is required. Track record of strong problem solving and organizational skills, attention to detail, and ability to multi-task. Strong written and oral communication skills Bonus Points If You Have (Preferred Requirements): Experience with Tecan or Beckman liquid handling platforms is preferred but not required. Experience with high content imaging and multiplex assay formats is preferred. Experience writing scripts to automate data processing or other coding experience is preferred. PHYSICAL/MENTAL REQUIREMENTS Requires work in BL2 laboratory environment with appropriate PPE Work Location Assignment: On Premise Last Day to Apply: January 22, 2026 The annual base salary for this position ranges from $60,200.00 to $97,500.00. In addition, this position is eligible for participation in client's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with client's Matching Contributions and an additional client's Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at client's Candidate Site - U.S. Benefits | (uscandidates.my**benefits.com). Compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Relocation assistance may be available based on business needs and/or eligibility. To find out more about Rangam, and this role, click the apply button. Satnam Singh SA Technical Recruiter | Rangam Consultants, Inc M: ************** E: *****************| W: **************

A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents Support method transfer, qualification of critical reagents, and other assay-related activities Participate in the review and basic trending of QC data Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking Collaborate with internal teams and external partners as part of cross-functional project support Contribute to investigations and deviation reports under guidance Perform other duties, as needed Qualifications: Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field Familiarity with basic Lab techniques and Data Analysis methods Strong organizational, communication, and interpersonal skills Detail-oriented and eager to develop problem-solving skills in a regulated lab environment Enthusiasm for learning and the ability to work both independently and within a team Desired Skills: Academic or internship experience with Mammalian Cell Culture and/or ELISAs

Industry: Pharmaceuticals Title: Quality Control Analyst II Duration: 11 months contract (+Possibility of extension) This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Description: The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness. Key Responsibilities' Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. Support weekend lab operations and maintain training records. Assist in lab equipment and inventory maintenance, including reagent and sample prep. Review data timely and qualify as a data reviewer. Perform operational assignments (raw material processes, environmental monitoring, in-process testing). Contribute to updating controlled documents (SOPs, work instructions, test methods). Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH). Participate in continuous improvement initiatives and cross-functional collaboration. Support regulatory submissions, inspection readiness, and audits Qualifications: B.S. in chemistry, biology, biochemistry, or related field. 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent. Experience in method transfer/implementation; understanding of method lifecycle management preferred. Strong technical writing, data analysis, problem-solving, and organizational skills. Excellent communication and teamwork. Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred

Quality Control Analyst II Norton 45 per hour This is an onsite role in Norton, MA. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Perform routine and non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies in accordance with SOPs Support weekend laboratory operations and maintain required training records Assist with laboratory equipment and inventory maintenance, including reagent and sample preparation Review data in a timely manner and serve as a qualified data reviewer Perform operational assignments such as raw material processing, environmental monitoring, and in-process testing Contribute to the creation and updating of controlled documents, including SOPs, work instructions, and test methods Follow internal policies, SOPs, and applicable regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration Support regulatory submissions, inspection readiness, and audits Qualifications Bachelor's degree in Chemistry, Biology, Biochemistry, or a related field 4-8 years of pharmaceutical or biotech experience in GMP QC or equivalent environments Experience with method transfer and implementation; understanding of method lifecycle management preferred Strong technical writing, data analysis, problem-solving, and organizational skills Excellent communication and teamwork abilities Proficiency in LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred

Title: QC Specialist - Chemistry Employment Type: Contract Status: Accepting Candidates About the role This role supports Quality Control Chemistry operations by leading QC Sample Management activities across multiple lab functions. You will ensure compliant, on-time sample processing while partnering with digital and quality teams in a fast-paced cGMP environment. Shift: Wednesday-Saturday, 6:00 AM-4:00 PM. Key Responsibilities • Lead QC Sample Management operations supporting Chemistry, Microbiology, Bioassay, and Raw Materials • Oversee daily schedules to ensure compliant sample processing and documentation • Author and maintain SOPs, deviations, CAPAs, and change controls • Act as primary support for audit readiness and regulatory inspections • Partner with Digital teams to optimize LIMS (LabVantage) and data workflows • Manage CTU systems, investigations, and compliance issue resolution Qualifications • BA/BS with 3-5 years or MS with 1-3 years of cGMP Quality Control experience • Strong hands-on experience with QC Sample Management • Proficiency with LIMS and Veeva Quality Systems • Working knowledge of FDA, EU, and ICH regulations • Experience with gowning, aseptic technique, and lab safety practices • Proven people management and cross-functional leadership skills Compensation (MA Pay Transparency): • Estimated hourly range: $40-$45/hr (W-2) • Final rate within this range will be based on skills, experience, and interview results.

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a hands-on, self-motivated Analytical Chemist to support New Product Development (NPD) and commercial product support across the ACP portfolio; ranging from metallization/plating chemistries to advanced packaging polymers and formulated materials. This role will lead development, implementation, and continuous improvement of analytical and characterization methods for specially synthesized raw materials (small molecules through complex polymers) and finished products, partnering closely with cross-functional stakeholders (DE, NPD, Manufacturing, Quality, and Technical Service) to enable scale-up, specifications, and customer support. Key responsibilities Analytical method development & execution: Develop, optimize, and run analytical/characterization methods for raw materials, intermediates, and formulated products supporting NPD milestones and commercial needs. Core techniques: Apply techniques such as CVS, HPLC/UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometry, and rheology (and related wet/physical methods). Other techniques relevant: ICP-OES/ICP-MS for metals/impurities, UV-Vis, FTIR, NMR, IC, TOC, DSC/TGA, particle size/zeta potential, SEM/EDS Method validation, transfer, and sustainment: Author/maintain methods, validation protocols/reports, and ensure robust method transfer to R&D and Manufacturing as needed. Data integrity & documentation: Maintain high-quality written documentation (methods, validation, batch/lot data packages, change control / MOC) and ensure traceable, audit-ready records. Troubleshooting & investigations: Support root-cause investigations, out-of-spec troubleshooting, and customer complaint response in collaboration with Quality/Manufacturing. Statistical/data analysis: Use statistical tools to analyze method performance, capability, trends, and investigation data (DOE, GR&R, SPC as applicable). Safety & teamwork: Work safely with hazardous chemicals in a collaborative, fast-paced lab environment; communicate clearly in both informal updates and formal presentations. Required qualifications Education: B.S. in Chemistry, Biology, Chemical Engineering, Materials Science, or related field. Experience: 3-5 years of hands-on experience in analytical chemistry supporting R&D/NPD, development engineering, manufacturing, or quality environments. (Experience characterizing small molecules, polymers, and/or inorganic/metal-containing chemistries is strongly valued.) Demonstrated ability to follow procedures with high repeatability, strong attention to detail, and commitment to safe lab practices. Strong written and verbal communication skills; able to translate data into clear technical conclusions and recommendations. Strong data analysis capability; JMP/Minitab (or similar) preferred. Preferred qualifications Demonstrated success developing/validating new analytical methods and supporting method transfer. Experience supporting semiconductor materials (e.g., plating baths, photoresists, dielectrics, silicones, packaging polymers) and working across interdisciplinary teams. Six Sigma (Green/Black Belt) or demonstrated experience applying structured problem-solving tools. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page. We use Artificial Intelligence (AI) to enhance our recruitment process.

About the Role The Small-Scale Cell Culture Scientist is a hands-on technical contributor in the Bioprocess Design Center (BDC), responsible for designing, executing, and documenting upstream cell culture experiments that generate high-quality technical evidence for Thermo Fisher Scientific's single-use bioprocessing technologies. This role operates at the intersection of experimental biology and systems-level process design. The successful candidate will independently own small-scale cell culture studies, translate experimental outcomes into actionable insights, and support integrated workflow development across upstream unit operations. While primarily lab-focused, the role requires strong communication skills and comfort engaging with cross-functional partners and customers. Location: This is an onsite position in Plainville, Massachusetts. Residency within commuting distance is required. No relocation assistance will be provided. Key Responsibilities Experimental Design & Execution Independently design and execute small-scale upstream cell culture experiments (typically 2L-50L) using single-use bioreactor systems. Incorporate process analytical techniques (PAT), online sensors, and at-line/off-line analytics to monitor and assess cell culture performance. Execute mammalian cell culture processes such as fed-batch and intensified workflows, ensuring reproducibility, data integrity, and traceability. Troubleshoot experimental and data-related issues, including sensor performance, data quality, and process variability. Systems, Automation & PAT enablement Analyze experimental datasets using advanced data analytics approaches, including multivariate analysis, trend analysis, and statistical methods, as appropriate. Leverage JUMP™ and other analytical programs to support data-driven decision making and improve experimental efficiency. Translate complex datasets into clear, defensible conclusions and visual summaries suitable for internal and customer-facing audiences. Author protocols, technical reports, summaries, and SOPs that integrate experimental outcomes with process data insights. Data Analysis & Digital Enablement Analyze experimental datasets using advanced data analytics approaches, including multivariate analysis, trend analysis, and statistical methods, as appropriate. Leverage JUMP™ and other analytical programs to support data-driven decision making and improve experimental efficiency. Translate complex datasets into clear, defensible conclusions and visual summaries suitable for internal and customer-facing audiences. Author protocols, technical reports, summaries, and SOPs that integrate experimental outcomes with process data insights. Collaboration & Communication Collaborate closely with engineers, scientists, and cross-functional teams to align experimental work with BDC priorities. Support customer visits, technical demonstrations, and internal reviews by clearly explaining experimental intent and results. Communicate progress, risks, and outcomes effectively to technical and non-technical audiences. Laboratory Operations & Compliance Maintain a safe, compliant, and organized laboratory environment. Follow applicable safety, quality, and data integrity requirements. Contribute to continuous improvement of lab workflows and experimental practices. Qualifications Education B.S. in Chemical Engineering, Biochemical Engineering, Biotechnology, Bioengineering, or a related field with 3+ years of relevant experience M.S. with 2+ years of relevant experience Equivalent combinations of education and experience will be considered Experience & Skills Hands-on experience with mammalian cell culture and upstream bioprocessing Familiarity with single-use bioreactor systems and small-scale process development Experience designing and executing controlled experiments; DOE experience preferred Strong data analysis, documentation, and technical writing skills Working knowledge of GLP/GMP concepts and laboratory best practices Proficiency with standard data analysis and reporting tools (e.g., Excel, PowerPoint) Preferred Attributes Demonstrated ability to work independently in a fast-paced, matrixed environment Strong problem-solving skills and attention to detail Ability to translate experimental data into practical insights Comfortable operating in environments with evolving requirements and priorities Collaborative mindset with a customer-centric orientation Physical Requirements Ability to work in a laboratory environment and handle light to moderate lifting (up to ~50 lbs) Standing and walking for extended periods during experimental execution Manual dexterity to operate laboratory equipment and instrumentation Why Join the Bioprocess Design Center The BDC is where Thermo Fisher technologies are stress-tested, validated, and transformed into real-world solutions for our customers. This role offers the opportunity to work hands-on with cutting-edge single-use systems, contribute to evidence that shapes customer confidence, and grow within a technically rigorous, highly collaborative environment. Compensation and Benefits The salary range estimated for this position based in Massachusetts is $96,000.00-$127,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Qualifications Compendial testing Additional Information If you or anyone from your connections is looking for a change; do call me on ************ or send me updated resume on gurupreet@mindlance(dot)com

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava ***********

Job Title: Quality Control (QC) Chemist (Metrology) FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range: $75,400 - $93,600 Purpose: The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, a combination of education, training, and special skills will determine the assignment of Level to a specific individual: Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: • Calibration and preventive maintenance of instruments. • Communications with vendors for installation, qualification and maintenance. • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head Education and Experience: • Bachelor's degree (BS or BA), physical sciences preferred • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets. • Working knowledge of Microsoft Office programs and other scientific based software. • Experience in Inhalation products (MDI) is a plus Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical requirements • Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required. • Able to wear appropriate personal protective equipment at all times, when required. • Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. Professional and Behavioral Competencies • Must be willing to work in a pharmaceutical packaging setting. • Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. • Must be willing to work some weekends based on business needs as required by management. • No remote work available • No employment sponsorship or work visas. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, apply with us today! Job Description We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development. We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects. Job Responsibilities and Requirements: Experience with protein chemistry, protein analytics, and bioprocess technology is required Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process Hands on experience and working knowledge on techniques including but not limited to liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet Hands on experience with SDS-PAGE, ELISA, and experience with protein purification/chromatography at the lab scale is a plus A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices Qualifications Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline BS 2-4 years or MS +0-2 years of relevant experience Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment Excellent skills in Microsoft Office, data analysis software, and other related applications Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Ability to think critically and demonstrate troubleshooting/problem solving skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information The position is full-time, on-site, Monday through Friday, 8:00 AM-5:00 PM. Pay range: $27.00 - $31.00 based on degree level and years of relevant experience Excellent full-time benefits including: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Piper Health & Sciences is seeking a full-time iPSC Production Scientist to join a growing organization's Bio/Engineering Production team onsite at their Massachusetts location. The ideal candidate will have a strong biology background and hands-on experience in iPSC stem cell culture, differentiation, and QC within a pharmaceutical or biotech environment. Responsibilities of the iPSC Production Scientist Include: * Full-time onsite schedule: Monday-Friday, 9:00 AM - 5:00 PM * Lead and support iPSC production and related lab activities * Perform hands-on stem cell culture and differentiation * Execute QC-related tasks in accordance with SOPs * Maintain accurate lab documentation and records * Support Bio/Engineering Production workflows * Follow all safety, GMP, and GLP standards Qualifications of the iPSC Production Scientist Include: * Biology degree is strongly preferred (Biomedical Engineering degrees are NOT a fit) * Proven hands-on experience with: * iPSC cell culture * Stem cell differentiation * Quality Control (QC) processes * Pharmaceutical or biotech industry experience preferred Compensation of the iPSC Production Scientist Includes: * Salary Range: $83,200.00 - $114,000.00 per year (equivalent to $40.00 - $55.00 per hour), based on experience and certifications. * Comprehensive Benefits: CIGNA Medical, Dental, Vision; 401k through ADP and sick leave as required by law. * Ability to work with a well renowned and growing organization that has a robust pipeline and quality culture. This job opens for applications on 1/12/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-AW1 #LI-ONSITE keywords: Scientist, iPSC Production, stem cell culture, induced pluripotent stem cells, cell differentiation, quality control, QC, laboratory scientist, cell biology, biotechnology, pharmaceutical production, bioengineering, GMP, GLP, SOP compliance, tissue engineering, regenerative medicine, bioprocessing, cell therapy, stem cell research, lab operations, onsite scientist, Medford MA jobs, contract scientist, PhD biology, master's biology, postdoctoral research, biotech scientist, pharma scientist, cell culture specialist, stem cell specialist, iPSC scientist, QC scientist, bio production scientist, laboratory techniques, cell-based assays, biotech careers, pharma careers, stem cell manufacturing, cell culture workflows, life sciences jobs, biopharma jobs, laboratory compliance, scientific documentation, biotech industry experience, pharmaceutical industry experience, cell line development, research scientist, production scientist, laboratory QC, stem cell differentiation protocols, cell culture maintenance, full-time onsite scientist, bioengineering production team, regenerative biology, tissue culture, cell therapy manufacturing, biotechnology research, pharmaceutical QC, biomanufacturing, cell biology techniques, stem cell QC testing, scientific method, laboratory safety standards, GMP compliance, GLP compliance, biotech contract role, scientist contract position, iPSC culturing, stem cell production, biotech Medford MA, pharma Medford MA, scientific careers, laboratory scientist jobs, cell therapy scientist, bioprocess scientist, QC laboratory scientist, stem cell lab work, biotech production workflows, pharmaceutical production workflows, life sciences contract jobs, biotech contract scientist, pharma contract scientist.

Job Title: Quality Control (QC) Chemist FLSA Classification: Full-Time, Exempt Professional Work Hours: General Shift: 8 AM - 5 PM (may vary based on business needs) Reports To: Quality Control Manager Pay Range: $65,000 - 90,000 (Annually) InvaGen pharmaceuticals is looking for talent in the following areas at our manufacturing site in Fall River, MA. Purpose The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience, or a combination of all three. Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual: Level 1: 0 to 3 years Level 2: 3 to 5 years Level 3: 5 to 10 years Senior: more than 10 years Level 2 or above is strongly preferred. Summary of Responsibilities: * Conduct routine testing or other analysis in a specific group or department setting * Conduct advanced testing and/or critical testing, as required. * Ensures QC Analysts receive proper training. * Attends meetings to keep informed of manufacturing priorities. * Ensures that safety standards are maintained. * Operate specialized equipment or conduct specialized skill testing. * Participate in investigation activities. * Ensure compliance to all data integrity and cGMP practices, procedures, and expect ensuring compliance with all good documentation practices. * Other duties and responsibilities as assigned by the Head of the Department or Section Head. Educational, Skills & Experience Requirements and Preferences: * Bachelor's degree (BS or BA), in Chemistry, Biology, Pharmaceutical Sciences, or related field, and a preferred 1-year experience in the pharmaceutical or biotechnology industries preferred. * Must have current Good Manufacturing Practices (cGMP) * Good Laboratory Practice (GLP) knowledge Professional and Behavioral Competencies * Proficiently speak, communicate, and understand (read and write) scientific work in English. * Have excellent organization, learning and teaching skills required to work in teams. * You enjoy working in a fast-paced environment and are flexible to changing requirements. * Working knowledge of raw materials and finished product testing and instruments and techniques such as GC, High-Performance Liquid Chromatography (HPLC), Karl Fischer (KF), Dissolution, Particle Size and ICP. * Lead Investigation activities * Familiarity with Chromatography systems is required, Empower is a plus. * Ability to understand and analyse complex data sets and must have working knowledge of Microsoft Office programs and other scientific based software. * Experience in Inhalation products (MDI) is a plus. * Effective interpersonal relationship skills and the ability to work individually and as a part a team. * Must be a detail-oriented self-starter, demonstrate initiative and possess a positive professional attitude towards work. * Must have strong organization and communication skills (written, verbal, and presentation). * Must be willing to work in a pharmaceutical packaging setting. * Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. * Must be willing to work some weekends based on business needs as required by management. * No remote work available Physical Requirements: * Work standing or walking unassisted for 75% or greater of an 8-hour period. * Unassisted lifting up-to 10 kg, may be required. * Able to wear appropriate personal protective equipment at all times, when required. * Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. Locations: Fall River, Massachusetts EEO Statement: Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Schedule: Sunday - Wednesday 6:00AM - 4:30PM Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

We are seeking a passionate PhD-level synthetic chemist to drive the discovery of small molecules for next-generation 3D printing resins. This position involves rapid exploration of chemical space through organic synthesis to develop photochemical and photophysical structure-property relationships. This role will be particularly appealing to chemists with a passion for both synthetic and physical organic chemistry. Our process uses a small amount of each lead candidate, so synthetic creativity is not limited by the scalability concerns that usually narrow the available chemical space in materials applications. Responsibilities Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. Characterize lead candidates via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. Contribute to the development of high-throughput analytical capabilities, small molecule databases, and virtual libraries. Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance. Mentor junior scientists. Maintain excellent electronic lab notebook documentation. Minimum Qualifications PhD in Organic Chemistry or BS in Chemistry and 5+ years of experience in a small molecule discovery role. Strong expertise in both synthetic and physical organic chemistry, demonstrated through publications and other activities. Significant experience designing and executing multi-step synthetic routes. Extensive experience with modern computing and data analysis tools relevant to synthetic chemistry. Excellent communication, organizational, and time management skills. Demonstrated ability to independently drive an idea from conception to project completion. Evidence of strong collaboration and teamwork talents/skills. Strong publication record, both as lead author and as contributor to other projects. Preferred Qualifications Expertise in photochemistry and/or radical chemistry. Significant experience with synthesis of heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. Experience with cheminformatics and/or computational chemistry tools (e.g. DFT) relevant to the production of structure-property relationships. Benefits We offer competitive compensation packages in our VC-backed startup. Benefits include a full suite of offerings covering medical, dental, vision and 401k plan. Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas. Highly collaborative work environment. Additional Information Travel: Occasional travel may be required from time to time Location: Boston, Massachusetts We value diversity in our company and are an Equal Opportunity Employer.

Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: We are seeking a highly motivated and skilled Analytical Scientist to join our Analytical team in New England. The successful candidate will have expertise in LCMS (Liquid Chromatography-Mass Spectrometry) based characterization of complex bioconjugates, with a strong understanding of ADC structure and stability. Core Responsibilities: Exercise technical judgment in the planning, implementation, and analysis of experiments related to method development, validation, reference standard creation and qualification, forced degradation, product characterization, and compatibility studies in accordance with pertinent ICH regulatory guidelines. Develop and optimize LCMS methods for qualitative and quantitative analysis of ADCs. Develop and validate quantitative LCMS methods such as: Drug-to-Antibody Ratio (DAR) determination. Payload quantification (free and conjugated forms). Linker stability and degradation profiling. Site-specific conjugation analysis. Perform intact mass analysis, peptide mapping, drug-to-antibody ratio (DAR) determination, and payload identification. Characterize ADCs for critical quality attributes including conjugation sites, linker stability, and degradation products. Author test methods, protocols, reports, and regulatory documents as needed. Provide support for development and cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards - including both in-process and release samples. Adhere to safety and quality standards. Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies. Collaborate with chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery. Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing. Possess strong communication (oral, written), organizational, and leadership skills. Maintain and troubleshoot LCMS instrumentation (e.g., Orbitrap, Q-TOF, Triple Quad). Qualifications: Required Ph.D., M.S., or B.S. in Analytical Chemistry, Biochemistry, Chemistry, Chemical/Biomedical Engineering, or other related scientific discipline. Relevant experience in analytical method development, validation and characterization of bioconjugates. (PhD with 4+ years, MS with 6+ years, BS with 8 + years of experience. 4+ years of hands-on experience in LCMS analysis of biologics, preferably ADCs. Strong knowledge of protein chemistry, conjugation technologies, and biotherapeutic development. Proficiency in any of the software tools for MS data analysis (e.g., Xcalibur, MassHunter, Skyline, Biopharma Finder). Well organized with good problem-solving skills, a high level of attention to detail and have a passion for delivering high quality data in a fast-paced environment. Preferred Experience with regulatory submissions and GMP/GLP environments. Experience with various techniques used in the characterization of ADC's such as capillary electrophoresis (CE-SDS) for ADC purity and size analysis, hydrophobic interaction chromatography (HIC) for DAR profiling, size-exclusion chromatography (SEC) for aggregation and stability studies, UV-Vis spectroscopy and fluorescence-based assays for payload quantification, and immunoassays (ELISA, ECL) for antibody detection. Salary Range: $100,000 - $120,000 annual base salary Our Commitment: Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava***********

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, apply with us today! Job Description We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development. We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects. Job Responsibilities and Requirements: Experience with protein chemistry, protein analytics, and bioprocess technology is required Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process Hands on experience and working knowledge on techniques including but not limited to liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet Hands on experience with SDS-PAGE, ELISA, and experience with protein purification/chromatography at the lab scale is a plus A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices Qualifications Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline BS 2-4 years or MS +0-2 years of relevant experience Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment Excellent skills in Microsoft Office, data analysis software, and other related applications Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Ability to think critically and demonstrate troubleshooting/problem solving skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information The position is full-time, on-site, Monday through Friday, 8:00 AM-5:00 PM. Pay range: $27.00 - $31.00 based on degree level and years of relevant experience Excellent full-time benefits including: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.