Manager, QC Microbiology, Cell Therapy

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary The Manager, QC Microbiology, is a highly critical role and is responsible for managing the QC Microbiology Laboratory which provides support to the CAR T manufacturing site. This department is responsible for microbiological related testing of in-process samples, final product testing, critical utilities sampling and testing, Validation and requalification support, incoming component testing, and microbiological identification. Sampling and testing must meet or exceed FDA, MHRA, PMDA, EU, and other governmental regulations or guidelines. The Manager QC Microbiology is responsible to act as the SME during regulatory inspections.

• PM Shift: Wednesday to Saturday 2 PM 12 AM

Duties/Responsibilities

• Manage QC Microbiology department.

• Management and coordination of the Microbiological Laboratory testing program and scheduling to ensure timely testing and results, to support final product testing and release, incoming components and materials testing and release, and monitoring of the critical utilities systems.

• Development and management of SOPs, forms, and methods required to support the compliant operation and testing conducted in the Microbiology laboratory.

• The Manager, QC Microbiology, plays a critical role in ensuring that all materials, products, methods and equipment are within specifications and ensuring accurate and timely disposition of test results and compliance investigations.

• Ensure that Microbiology lab test results which exceed the specification limits, are submitted as a Deviations in the eQMS system, investigated, and effective CAPAs are implemented.

• Ensure the site and department objectives are met.

• Manage and develop direct reports.

• Management and scheduling of Microbiology laboratory personnel within the department to meet the Manufacturing schedule and needs.

• Ensure employees are properly trained and qualified to perform assigned tasks, provide performance evaluations and support career development of direct reports.

• Perform other tasks as assigned.

Job Safety Requirements and Essential Physical Demands The Manager role is responsible for supporting and training staff on activities that may include the following:

• Ability to perform lifting tasks up to 20 lbs (9 kg) at floor and waist height. Ability to lift up to 10 lbs (4.5 kg) overhead as well as push or maneuver carts to transport materials between locations.

• Ability to perform frequent pipetting and related laboratory tasks within a biological safety cabinet, including extended periods of seated work.

• Ability to independently don, doff, and wear required personal protective equipment such as but not limited to lab coat/frock, gloves, safety glasses/face shield for prolonged periods while performing laboratory work.

• Ability to safely handle and use chemical disinfectants, flammable materials, and hazardous chemicals.

• Work may involve handling of dry ice, liquid nitrogen, and cryogenically cooled materials.

• Ability to use step stools while reaching and handling materials.

• Ability to work in a Biosafety Level 2 (BSL-2) environment.

Qualifications Education and Experience:

• Bachelor’s degree required, preferably in Microbiology or related science.

• Advanced degree preferred.

• 7 years’ relevant work experience required, preferably in a Microbiology laboratory and/or Environmental Monitoring. Experience working with cell therapy products are preferred.

• 2 years of leadership experience preferred.

• Must have experience in supporting sterile compounding and filling operations.

• Experience in participating and supporting regulatory audits preferred: FDA, MHRA, PMDA, and TGA.

• Experience in working with Quality Systems preferred: SOPs, Change Control, Deviations, CAPAs, and Risk Assessments.

• An equivalent combination of education or experience may substitute.

REQUIRED COMPETENCIES:

• Advanced knowledge of cGMPs, FDA, USP, MHRA, BP, EP, JP, PMDA, and DEA regulations and guidelines, as related to manufacture of cell therapy products.

• Advanced data integrity knowledge and practices.

• Intermediate understanding of statistics, control charts, action and alert limits.

• Advanced knowledge of Microbiology, media, incubation conditions, microorganism isolation, identification, and enumeration techniques, validations/suitability studies etc.

• Intermediate knowledge of Good Engineering Practices and Validation Principles: URS, IQ, OQ, PQ, PVs, etc.

• Ability to lead and maintain the development of Microbiology laboratory testing data and trending.

• Advanced verbal and written communication skills.

• Demonstrated critical reasoning, problem solving, troubleshooting, investigation, and decision-making skills.

• Must be team-oriented and have the demonstrated ability to work cross departmentally throughout the manufacturing site.

• Demonstrated leadership and management skills, including establishing direction and goals, and guiding execution while fostering a team-based environment.

• Advanced mentoring and coaching, influencing, negotiating and personal interaction skills.

• Demonstrated resource management and planning skills. Must be flexible and adaptable, and able to work under pressure, while meeting designated timelines.

• Advanced knowledge of safety, OSHA, and EPA regulations. Electrical and energized equipment (lockout/tag out), fall safety, HAZCOM, MSDS sheets, etc.

• Advanced of Microsoft Word, Outlook, Excel, PowerPoint, etc

WORKING CONDITIONS:

• The incumbent will be required to work in an office and Microbiology laboratory environment.

• The incumbent will be required to gown for entry into Aseptic core and supporting areas, on an as-needed basis.

• The management incumbent (or designee) will be expected to be on call, to support manufacturing issues involving sampling and/or test excursions or questions during shift operations.

• Occasional travel may be required.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Devens - MA - US: $100,490 - $121,767

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.

Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

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R1607182 : Manager, QC Microbiology, Cell Therapy