Associate, QC Analytical, Cell Therapy

Bristol Myers Squibb • Devens, MA

1d • $37 - $45 • Onsite

About The Position

The Associate, QC Analytical, Cell Therapy supports quality-control testing of in-process, final product, and stability samples. The role may also assist with documentation, data verification, deviations, investigations, CAPA-related tasks, and continuous improvement efforts. The position reports to QC management and may include training analysts on general job duties.

The role applies scientific principles to analytical testing and proper laboratory-equipment use. The successful candidate follows procedures accurately, communicates effectively with peers and management about work completion and needs, and works collaboratively in a fast-paced environment to prioritize tasks and meet deadlines.

Requirements

• Ability to accurately and completely understand and follow procedures.
• Ability to apply scientific principles to analytical testing and proper use of laboratory equipment.
• Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
• Attention to detail and demonstrated organizational skills.
• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
• 0–2+ years of relevant analytical testing or QC experience, or an equivalent combination of education and experience; preferably in a regulated environment.

Nice To Haves

• Bachelor’s degree in science preferred; an associate’s degree with an equivalent combination of education and work experience may be considered. For Netherlands roles, a bachelor’s degree/HLO in (bioanalytical) science is preferred; MLO level 4 with an equivalent combination of work experience may be considered.
• Prior experience with cell and molecular biology techniques, such as cell-based assays, flow cytometry, qPCR, or aseptic technique, is preferred.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Review GMP documentation and perform data verification, as needed.
• Support document revisions, projects, CAPA and deviation/investigation-related tasks, and continuous improvement efforts.
• Train analysts on general job duties, as needed.
• Perform other tasks as assigned.

Benefits

• Comprehensive benefit plans, including wellbeing support, retirement and financial protection benefits, and medical, dental, vision, life, and disability insurance offerings, subject to plan terms and eligibility.
• Eligible U.S.-based exempt employees receive Flexible Time Off without a set accrual limit, subject to manager approval, and 11 paid company holidays each year.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires, subject to manager approval, 11 paid company holidays, and 3 optional holidays.
• Depending on eligibility, additional time-off benefits may include paid sick leave, up to two paid volunteer days per year, summer-hours flexibility, and leaves for medical, personal, parental, caregiver, bereavement, or military needs.
• Eligible employees may receive an annual Global Shutdown between Christmas Day and New Year’s Day.
• Eligible employees may have access to additional discretionary incentive cash and stock opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level