Job was saved successfully.
Job was removed from Saved Jobs.

Job Details

Bristol-Meyers Squibb, Co.

Manager, Quality Control Microbiology CAR-T



Full Time

On Site


Summit, New Jersey, United States

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Purpose and Scope of Position

The Manager, QC Microbiology supervises and oversees the activities and personnel in the microbiology group as they perform routine EM (Environmental Monitoring) Sterility, Growth Promotion, EM plate reads, Endotoxin, Mycoplasma, and non-routine microbiological testing and activities to support Aseptic Process Simulations, In-process EM, EM Performance Qualifications, Gowning Qualifications, Aseptic Operator Qualifications and contamination control activities in support of CAR T manufacturing operations. Trends data, prepare metrics, reviews documents, reviews procedures, protocols/reports, support investigations and works on CAPAs. The Manager may be required to be hands on and perform lab tasks/testing as needed. The Manager performs responsibilities independently in accordance with the BMS’s policies, procedures, and state, federal and local laws and ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other regulatory guidelines/requirements at all times.

Duties and Responsibilities

  • Mentor lab personnel as needed.
  • Ensure employees assigned to tasks are properly trained.
  • Complete performance evaluations and take additional action as needed.
  • Support career development of direct reports.
  • Foster a positive and inclusive work environment.
  • Oversee personnel’s work schedule to ensure all assigned tasks are performed in a timely manner
  • Perform data review and additional laboratory activities when needed.
  • Ensure laboratories remain in an audit ready state.
  • Utilize scientific principles to assist in troubleshooting and problem solving for deviations.
  • Support special projects.
  • Serve as author and/or technical reviewer of departmental SOPs and other technical documents.
  • Write and review protocols and reports.
  • Communicate with department and cross-functional management.
  • Perform other duties as assigned.

Required Competencies:

Education and Experience

  • Bachelor’s degree required, preferably in Microbiology or a related science.
  • 7-10 years’ relevant work experience required, preferably in a Quality Control Microbiology or Environmental Monitoring team in a pharmaceutical manufacturing environment with cGMP requirements.
  • Minimum of 1-2 years of people management experience required.
  • QC Microbiology/EM experience is required.
  • Cell and gene therapy experience preferred.
  • Experience with Aseptic Process Simulations, EM Performance Qualifications, Gowning Qualifications and contamination control activities preferred.
  • An equivalent combination of experience/education is acceptable.

Knowledge, Skills, and Abilities

  • Ability to interact with regulatory agencies and internal auditors.
  • Flexibility with working hours, ability to multi-task and work well under tight timelines.
  • Advanced knowledge of current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory guidelines/requirements.
  • Ability to interpret and write complex documents.
  • Advanced written, verbal, and interpersonal communication skills.
  • Advanced knowledge/experience with MS Word, Outlook, Excel, MS PowerPoint, Visio, LIMS.
  • Advanced understanding of data integrity and good documentation practices.
  • Strong problem-solving, troubleshooting skills, critical reasoning and decision-making skills.
  • Strong organization and time management skills.
  • Strong team spirit, work ethics and accountability.
  • Able to develop and motivate others; delegate and solve routine problems.
  • Ability to gown and maintain an aseptic work environment.
  • Ability to prioritize tasks and escalate issues as required.

Working Conditions

  • This position may include standing, bending, reaching, kneeling, balancing, pushing, pulling, lifting or carrying (not more than 25lbs).
  • This position requires concentrating, analytical thinking, working under tight timelines, decision making, and adapting to change.
  • This position may require working within controlled environments with defined gowning requirements.
  • This position requires working around magnetic fields and radio frequencies.
  • This position requires additional gowning/PPE to work in manufacturing, warehouse, and laboratory environments.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.