Manager, Manufacturing

Bristol Myers Squibb EU Policy; Bothell (WA); On-site; USD 114,000 - 138,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Medical/dental/vision insurance

Job summary

Bristol Myers Squibb in Bothell, WA is seeking a Manufacturing Manager I to lead and drive the execution of cGMP cell therapy manufacturing processes, mentoring a team and guiding cross-functional collaboration to ensure safety, compliance, and reliable production.

You will manage SOPs, batch records, change controls, MRB activities, training, and continuous improvement, while maintaining inspection readiness and working in a highly regulated environment.

Qualifications

• 5+ years in cGMP cell therapy manufacturing or related field with 2 years of leadership experience (lead or equivalent).
• Experience in cell therapy manufacturing and aseptic processing.
• Proven performance management responsibilities.
• Knowledge of Change Controls and MRB processes.
• Ability to write and review GMP documentation and training materials.

Responsibilities

• Manage creation and compliance of Source Governing Documents related to cell therapy operations.
• Oversee operations within validated manufacturing systems.
• Plan, resource, and oversee daily activities while controlling costs.
• Maintain clean, compliant, inspection-ready facilities and equipment.
• Drive right-first-time initiatives and address compliance issues.
• Lead change controls, deviations, and investigations to closure.
• Develop corrective/preventive actions and CAPA programs.
• Ensure training and GMP compliance for all staff.
• Hire, mentor and develop personnel and conduct performance reviews.

Skills

Leadership

Troubleshooting

Performance management

Teamwork

Data analysis

Education

Bachelors in science or engineering

Job description

SHIFT OPTIONS

Days – Sun – Tue (alt. Wed) 0500 – 1730

Days – Thu – Sat (alt. Wed) 0500 – 1730

Swing – Sun – Tue (alt. Wed) 1100 – 2330

Swing – Thu – Sat (alt. Wed) 1100 – 2330

Nights – Sun – Wed (alt. Sat) 1700 – 0530

Nights – Wed – Fri (alt. Sat) 1700 – 0530

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.

Position Summary

The Manufacturing Manager I leads and drives the execution of manufacturing processes according to established electronic work instructions and production records for the manufacture of cell therapies with Current Good Manufacturing Practices (cGMP’s). The Manager I is responsible for leading a team whose primary focus is on execution of manufacturing processes, technical assessment of processes, and driving a culture of safety, compliance, and innovation within their functional group. The Manager I plays a crucial role in guiding personnel in their group with technical expertise to lead troubleshooting activities, provide investigation support, analyze process/equipment data, and identify and implement process improvements. This role also creates an environment that fosters idea generation, team and cross-functional collaboration, and execution of success, repeatability, and reliability of process and staff.

Duties/Responsibilities

• Manages the creation, implementation and compliance of all Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms) related to cell therapy operations for self and others

• Oversee operations within the requirements of a validated manufacturing system(s)
• Plan, assign resources and oversee daily operational activities associated with assigned areas of responsibility while controlling costs
• Maintain operating and storage areas to ensure that they are compliant, efficient, effective, safe and always inspection ready
• Drives right-first-time initiatives and holds team accountable for compliance performance. Generates solutions for compliance issues.
• Prepares, gains alignment and implements Change Controls
• Completes MRB slides and presents at MRB meetings as needed
• Initiates change controls, notice of events, deviations and investigations and drives actions to closure as assigned
• Evaluates team performance and drives continuous improvement of cost, quality, safety, culture and delivery.
• Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions, deviation responses and investigations
• Verify manufacturing associates and team leads are fully trained on respective curricula to maintain compliance prior to performance any GxP task.
• Create 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, including psychological safety, and the safety of the patients by compliance with company procedures and policies, and cGMP requirements
• Efficiently coordinate, communicate, and provide Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner and in accordance with schedules and defined implementation timelines
• Presence in the cell therapy manufacturing facility to participate in walk throughs, provide process troubleshooting, participate in event triages, and have direct contact with manufacturing personnel in order to provide timely, effective coaching.
• Oversee operators on daily basis as they:
• Perform unit and support operations described in Source Governing Documents in a safe and GMP compliant manner
• Complete documentation contemporaneously required by Source Governing Documents.
• Maintain training compliance by completing all training assignments to ensure the necessary technical skills and knowledge
• Assist in the setup of manufacturing areas and equipment/fixtures, facility and equipment commissioning, and qualification and validation activities
• Write manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements
• Hire, mentor and develop exceptional people. Conduct effective performance reviews with supporting documentation and identify opportunities for career growth for manufacturing associates. Immediately address performance issues through document coaching / feedback as required.

Reporting Relationship

Sr. Manager or Associate Director

Education

• Bachelors in relevant science or engineering discipline, or equivalent in work experience

Experience

• 5+ years of experience in cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience with 2 years leadership experience (i.e. lead or equivalent) including performance management responsibilities is highly desirable
• Experience in the following is highly preferred:
• Cell therapy manufacturing
• Aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human derived materials in BSL-2/ML-1 containment areas.
• Cell expansion using incubators and single use bioreactors, Cell washing processes, Cell separation techniques and cryopreservation processes and equipment.

Working Conditions

• Must be able to stand/walk for extended periods of time.
• Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as needed), which require gowning and personal protective equipment (PPE), including by not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protection.
• Required to carry and/or lift up to 30 pounds, 15 kg, several times a day, while handling production equipment and/or materials.
• Required to push and/or pull up to 50 pounds, 25 kg, several times a day, while handling production equipment and/or materials.
• Work is areas that may have strong magnets.
• Must be able to work in a BSL2 / ML-1 work environment handling human blood components
• Work in areas with exposure to vapor phase liquid nitrogen
• Must be able to work assigned shift (Day, Evening, Night, Weekends and/or Holidays)

Compensation Overview

Bothell - WA - US: $113,930 - $138,051

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 [e-mail]. 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/

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.