Senior Specialist, QC Analytical, Cell Therapy
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Working with Us
Challenging. Meaningful. Life‑changing.
Working at Bristol Myers Squibb brings uniquely interesting work every day – from optimizing a production line to launching breakthroughs in cell therapy. The work transforms patients’ lives and the careers of those who do it. Grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible. Position Summary
Responsible for supporting QC testing for in‑process, final product, and stability samples. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Key Responsibilities
Perform method transfer/validation and routine testing of in‑process, final product, and stability samples. Anticipate and perform routine troubleshooting and problem solving with minimal guidance. Perform data verification, data review and review of GMP documentation for general and complex methods. Perform document revision, project, CAPA and deviation/investigation related tasks and continuous improvement efforts. Train and mentor others on QC test methods, processes and procedures. Perform other tasks as assigned. Qualifications & Experience
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. Demonstrated technical writing skills. High problem‑solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs. Ability to work in a fast‑paced team environment, meet deadlines, and prioritize work. Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred. Education & Experience
Bachelor’s degree or equivalent required, preferably in science. 4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment. Demonstrated experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, and aseptic technique). Compensation Overview
Devens – MA – US: $43.84 – $53.12 per hour. The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Benefits
Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well‑being and Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Equal Employment Opportunity Statement
Bristol Myers Squibb is an Equal Employment Opportunity/affirmative action employer and encourages qualified applicants with diverse backgrounds to apply. Each BMS facility is an EEO/affirmative action employer and no applicant or employee is required or encouraged to provide a pregnancy, medical or disability status for any hiring or employment decision. The BMS EEO statement is available at https://careers.bms.com/eeo.
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Challenging. Meaningful. Life‑changing.
Working at Bristol Myers Squibb brings uniquely interesting work every day – from optimizing a production line to launching breakthroughs in cell therapy. The work transforms patients’ lives and the careers of those who do it. Grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible. Position Summary
Responsible for supporting QC testing for in‑process, final product, and stability samples. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Key Responsibilities
Perform method transfer/validation and routine testing of in‑process, final product, and stability samples. Anticipate and perform routine troubleshooting and problem solving with minimal guidance. Perform data verification, data review and review of GMP documentation for general and complex methods. Perform document revision, project, CAPA and deviation/investigation related tasks and continuous improvement efforts. Train and mentor others on QC test methods, processes and procedures. Perform other tasks as assigned. Qualifications & Experience
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. Demonstrated technical writing skills. High problem‑solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs. Ability to work in a fast‑paced team environment, meet deadlines, and prioritize work. Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred. Education & Experience
Bachelor’s degree or equivalent required, preferably in science. 4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment. Demonstrated experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, and aseptic technique). Compensation Overview
Devens – MA – US: $43.84 – $53.12 per hour. The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Benefits
Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well‑being and Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Equal Employment Opportunity Statement
Bristol Myers Squibb is an Equal Employment Opportunity/affirmative action employer and encourages qualified applicants with diverse backgrounds to apply. Each BMS facility is an EEO/affirmative action employer and no applicant or employee is required or encouraged to provide a pregnancy, medical or disability status for any hiring or employment decision. The BMS EEO statement is available at https://careers.bms.com/eeo.
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