Specialist, QC Analytical, 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 a Specialist, QC Analytical, Cell Therapy at the Cell Therapy Facility (CTF) in Devens, MA.  The QC Specialist is responsible for supporting Quality Control bioanalytical testing for method validation, critical reagent qualification, in-process, release, and stability testing of clinical and commercial cell therapy drug product.  This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot.  Additionally, the QC Specialist may assist with assay transfer.

Shifts Available:

Wednesday - Saturday, 6am – 4pm, onsite

Responsibilities:

• Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
• Use scientific principles to assist with analytical testing methods and the proper use of laboratory equipment.
• Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
• Review all data in accordance with applicable procedures and cGMP requirements.
• Anticipate and troubleshoot problems.  Communicate effectively with management regarding task completion, roadblocks, and needs.
• Train new analysts to general job duties.
• Support document revision, project, CAPA, and investigation/deviation related tasks.
• Perform assigned tasks within a CAPA, deviation, or project.
• 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:
  • AM Shift:Wednesday to Saturday 6 AM – 4 PM

Knowledge Skills and Abilities:

• Hands on experience with various bioanalytical techniques (cell-based assays, flow cytometry, ELISA, qPCR).
• Scientific knowledge in the characterization, validation and transfer of bioanalytical methods preferred.
• Ability to understand, follow, interpret and apply Global Regulatory and cGMP requirements accurately and completely.
• Technical writing skills.
• Problem-solving ability/mentality, technically adept and logical.
• Ability to work in a high-paced team environment, meet deadlines, and prioritize work.
• Ability to communicate effectively with peers, department management and cross-functional peers.
• Knowledge of LIMS and laboratory data analysis systems preferred.

Basic Requirements:

• Bachelor’s degree required, preferably in science. Advanced degree preferred.
• 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 $83,290 - $100,900, plus incentive cash and