Associate, QC Analytical Flow Cytometry, A2 Shift, Cell Therapy

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Position Summary

Bristol Myers Squibb is seeking a QC Associate to join our QC Analytical Flow Cytometry team at the Cell Therapy Facility (CTF) in Devens, MA.  The QC Associate is responsible for supporting Quality Control bioanalytical testing for in-process, release, and stability testing of clinical and commercial cell therapy drug product.  Additionally, the QC Associate may assist with investigations and continuous improvement efforts.  The QC Associate role is stationed in Devens, MA and reports to the Manager, QC Analytical for the Devens CTF.

This position works the following shift schedule: PM Shift: Sunday to Wednesday 2 PM – 12 AM.

Key Responsibilities

• Perform bioanalytical testing and data review of in-process, batch release, and stability samples of cell therapy drug product in accordance with applicable procedures and cGMP requirements.

• Ensure timely completion of testing and tasks as assigned.

• May train on additional test methods and provide support to a broader spectrum of testing responsibilities.

• Support investigations through data gathering or interview process.

• Apply scientific principles to analytical testing and the proper use of laboratory equipment.

• Communicate effectively with management regarding task completion, roadblocks, and needs.

• May participate in projects and continuous improvement efforts.

• Perform other tasks as assigned.

• Support for QC and manufacturing operations requires shift coverage consisting of weekdays, weekends, holidays, and during adverse weather conditions. 

Education & Experience

• Bachelor’s degree required, preferably in the physical or life sciences.

• 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.

• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.

• Prior experience in cell and molecular biology techniques (cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

• Knowledge of regulatory standards as they apply to GMP laboratories is preferred. 

• Attention to detail and demonstrated organizational skills.

• Knowledge of basic electronic systems (email, MS Office, etc.) required.

• Experience with LIMS and ELN computer applications preferred.

• Ability to work in a high-paced team environment, meet deadlines, and prioritize work.

• Ability to communicate effectively with peers and department management.

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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-es