QC Analytical Manager, Molecular, Cell Therapy in Devens, MA

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Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: 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 theres no better place than here at BMS with our Cell Therapy team.

Bristol Myers Squibb is seeking a Manager QC Analytical Molecular at the Cell Therapy Facility (CTF) in Devens MA. This role will manage the daily operations of the QC Analytical shift responsible for QC bioanalytical testing and data review for in-process release and stability testing of clinical and commercial cell therapy drug product. The Manager QC Analytical will also be responsible for hiring mentoring and developing the QC Analytical team to support business operations and employee career development.

Shifts Available:

Wed Sun 6am 2pm

Responsibilities:

• Supervise the QC Analytical lab staff on shift and oversee the daily lab activities related to in-process final release and stability testing of cell therapy drug product.
• Develop and execute a work plan for the shift ensuring safety quality and performance targets are achieved.
• Perform QC data review ensuring results are compliant with specifications and regulations. Report abnormalities.
• Track trend and report key performance metrics. Drive continuous improvement in the lab to increase productivity and efficiency. May collaborate with other departments to identify and implement process improvements.
• Review and approve test methods and procedures to ensure operational alignment and compliance with corporate policies and procedures.
• Own and evaluate relevant change controls investigations deviations CAPAs.
• Hire mentor and develop team members to support the business operations and employee career development.
• Oversee training of the team members.
• Communicate effectively with management regarding task completion roadblocks and needs.
• Responsible for cGMP compliance in all aspects of laboratory operations. Participate in site team supporting and managing regulatory inspections and findings.
• Perform other tasks as assigned.

Knowledge Skills Abilities:

• Experience with various bioanalytical techniques (cell-based assays ELISA qPCR flow cytometry) and associated equipment.
• Experience with laboratory LIMS ELN and ERP systems (e.g. SAP) preferred.
• Ability to work in a highly regulated environment and follow regulatory requirements and GMPs.
• Ability to mentor associates manage multiple assignments while meeting timelines in a GMP environment.
• Advanced ability to work collaboratively in a high-paced team environment meet deadlines and prioritize work from multiple projects.
• Excellent organizational and critical thinking skills.
• Advanced problem-solving ability/mentality technically adept and logical.
• Advanced ability to communicate effectively with peers department management and cross functional peers.
• Proficient with Excel Visio PowerPoint and other common software applications.
• The incumbent will be working around biohazardous materials.

Minimum Requirements:

• Bachelors degree required preferably in Chemistry Microbiology or related science.
• 6 years of relevant laboratory work experience preferably in a regulated environment.
• 2 years of management and people leader experience.
• An equivalent combination of education and experience may substitute.

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Compensation Overview:

Devens - MA - US: $99380 - $120428

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job such as required skills where the job is performed the employees work schedule job-related knowledge and experience. Final individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit 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 programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability life insurance supplemental health insurance business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays Global Shutdown Days between Christmas and New Years holiday up to 120 hours of paid vacation up to two (2) paid days to volunteer sick time off and summer hours flexibility. Parental caregiver bereavement and military leave. Family care services such as adoption and surrogacy reimbursement fertility/infertility benefits support for traveling mothers and child elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

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 a supportive culture promoting global participation 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 an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

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Required Experience:

Manager