Associate, QC Analytical - Flow Cytometry, Cell Therapy in Devens, MA

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.

Bristol Myers Squibb is seeking an Associate, QC Analytical – Flow Cytometry, Cell Therapy 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.

Shifts Available:

Sunday – Wednesday, 2pm – 12am

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

Knowledge and Skills:

• 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.

Basic Requirements:

• 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.

The starting compensation for this job is a range from $74,510-$90,300, plus incentive cash and stock opportunities (based on eligibility).

The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.

Final, individual compensation will