Scientist, QC Analytical, Cell Therapy
Bristol Myers SquibbAbout the role
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.
Please note: Relocation assistance and visa sponsorship are not available for this position.
Position Summary: The Scientist position is responsible for supporting routine testing of samples in Quality Control for the Bristol Myers Squibb (BMS) CAR T Manufacturing facility located in Summit, NJ in accordance with BMS policies, standards, procedures and Global Regulatory and cGMP requirements. As the subject matter expert (SME) of the
commercial methods, the Scientist will be responsible for working independently for
QC lab method support, troubleshooting, and training.
Duties/Responsibilities:
• Subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples.
• 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 (general and complex) and/or 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.
Qualifications Specific Knowledge, Skills, Abilities:
• Ability to accurately and completely understand, follow, interpret, and apply
Global Regulatory and cGMP requirements.
• Demonstrated technical writing skills.
• High problem-solving ability/mentality, 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.
Education/Experience/Licenses/Certifications:
• Bachelor’s degree or equivalent required, preferably in Science. Advanced
degree preferred.
• 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).
The starting compensation for this job is a range from $$91,000 - $114,000, 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 the geographic location where work is performed. Final, individual compensation is decided commensurate with demonstrated experience. For more on benefits, please visit our BMS Careers Site. Eligibility for specific benefits listed therein may vary based on job and location.
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance p
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