Associate Scientist, Quality Control Analytical; 3rd Shift

Position Summary

Subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples. Perform data review/verification, complex troubleshooting, and method training. Own project, document revisions, deviations/investigations/CAPA, and continuous improvement efforts.

• Perform review of testing data (e.g., data packets, final lot file, COA review).
• Anticipate and perform complex troubleshooting and problem solving independently.
• Perform data verification, data review and review of GMP documentation for multiple methods and products.
• Own project, CAPA and deviation/investigation related tasks and/or continuous improvement efforts.
• May represent the department in regulatory inspections (internal and external audits).
• Train and mentor others on multiple QC test methods, processes and procedures.
• Cross trained on multiple complex analytical methods and/or multiple products.
• Author and review/revise technical documents such as test methods, SOPs, specifications, trend reports and/or sample plans as appropriate.
• Perform other tasks as assigned.

This position will report to QC management.

• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
• Demonstrated technical writing skills.
• High problem‑solving ability, technically adept and logical.
• Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs.
• Advanced ability to work in a fast‑paced team environment, meet deadlines, and prioritize work from multiple projects.
• Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.
• Strong mentoring, coaching, influencing, negotiating and personnel interaction skills.
• Bachelor’s degree or equivalent required, preferably in science. Advanced degree preferred. PhD in bioanalytical science preferred in Netherlands.
• 6+ 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).

Summit West - NJ - US: $92,880 - $112,548. The starting compensation range for this role is listed above for a full‑time employee basis. Additional incentive cash and stock opportunities may be available. Final, individual compensation will be decided based on demonstrated experience.

Health coverage and support:
Medical, pharmacy, dental, vision, wellbeing programs, 401(k) plan, disability, life insurance, supplemental health insurance, travel protection, personal liability protection, identity theft benefit, legal support, survivor support.

Paid Time Off: US Exempt Employees flexible time off (unlimited, with manager approval, 11 paid national holidays). Phoenix, AZ, Puerto Rico and Rayzebio exempt employees: 160 hours annual paid vacation, 11 national holidays, and 3 optional holidays. Additional time off may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

BMS is an equal opportunity employer. We consider qualified applicants with arrest and conviction records per applicable laws. We are dedicated to ensuring people with disabilities can excel through a transparent recruitment process, reasonable accommodations, and ongoing support. Contact  for accommodations.

R1601699 :
Associate Scientist, Quality Control Analytical (3rd Shift)