Manager, Cell Therapy Manufacturing in Devens, MA

Bristol-Myers Squibb Company

Harvard (MA)

On-site

USD 105,000 - 127,000

Full time

3 days ago
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Benefits offered by this job

Flexible Time Off
Vacation time

Job summary

Bristol Myers Squibb is seeking a Manager, Cell Therapy Manufacturing for Devens, MA. The role leads the 24/7 manufacturing operations for clinical and commercial products, ensuring adherence to cGMP, safety and quality standards.

The position oversees staffing, training and continuous improvement in a high-complexity cell therapy environment. The role requires extensive experience in cell therapy manufacturing, aseptic processing, and strong leadership skills to mentor teams, manage deviations,

Qualifications

  • 5+ years of experience in cGMP bioprocessing manufacturing or cell therapy manufacturing.
  • Experience with aseptic processing in ISO 5 biosafety cabinets and handling human-derived materials in BSL-2 containment.
  • Bachelor’s in a relevant science or engineering discipline, or equivalent experience.

Responsibilities

  • Support manufacturing documentation, procedures and policies.
  • Oversee daily operations for assigned areas in a 24/7 cell therapy unit.
  • Maintain compliant, safe and efficient operating and storage areas.
  • Identify issues and drive corrective and preventative actions and investigations.
  • Foster teamwork, safety and compliance with cGMP requirements.
  • Coordinate with Planning, Quality Assurance and Global Supply to communicate status.

Skills

Cell therapy manufacturing
cGMP bioprocessing
Aseptic processing
BSL-2 material handling
Leadership/mentoring

Education

Bachelor's degree in science or engineering

Job description

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.

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.

The Manager, Cell Therapy Manufacturing supports the commercial operations of the facility. The Manager will be responsible for the people manufacturing both clinical and commercial product with oversight of shifts that cover 24/7 cell therapy manufacturing unit operations such as media preparation, cell selection, cell processing, or product fill, all of which are executed in accordance with Current Good Manufacturing Practices (cGMP’s).

Shifts Available:

6am – 6pm, rotating schedule including holidays and weekends

Responsibilities:
  • Supporting the development, implementation and compliance of manufacturing documentation, procedures and policies.
  • Operating within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility.
  • Maintaining operating and storage areas that are compliant, efficient, effective and safe.
  • Identifying strategic and operational issues to prevent deviations and maintain a compliant environment. Leading and managing the development of corrective and preventative actions, deviation responses and investigations.
  • Creating an environment of teamwork, open communication, and a sense of urgency. Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements.
  • Efficiently coordinating, communicating, and providing Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner in accordance to schedules and defined implementation timelines.
  • Overseeing operators on daily basis as they:
    • Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner.
    • Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
    • Maintain training assignments to ensure the necessary technical skills and knowledge.
    • Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification and validation activities.
  • Hiring, mentoring and developing exceptional people
  • Conducting performance reviews and identifying opportunities for career growth for manufacturing associates.
Working Conditions:
  • This position will require shift work, including holidays and weekends.
  • This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets.
Knowledge, Skills & Abilities:
  • Experience in cell therapy manufacturing techniques, including cell washing processes, cell separation processes, cryopreservation processes, cell expansion processes using incubators and bioreactors, and automated equipment is highly preferred.
  • Experience with aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas is highly preferred.
Minimum Requirements:
  • 5+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.
  • Bachelors in relevant science or engineering discipline, or equivalent in work experience.

BMSCART #LI-ONSITE

Compensation Overview:

Devens - MA - US: $104,975 - $127,205

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/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1608452 : Manager, Cell Therapy Manufacturing in Devens, MA

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