Manufacturing Cleaning

2 weeks ago

Bothell WA USA, United States Bristol Myers Squibb Full time
About the Role

Bristol Myers Squibb is seeking a highly skilled and experienced Manufacturing Cleaning & Sanitization Manager to join our team. As a key member of our operations team, you will be responsible for leading and driving the execution of routine and on-demand facility cleaning and sanitization to support the manufacture of cell therapies with Current Good Manufacturing Practices (cGMP's).

Key Responsibilities
  • Provide direct oversight of the completion of daily activities that contribute to cleaning and sanitization of GMP areas for CAR-T therapy manufacturing.
  • Act as an area/system owner, a point of contact for all work to be carried out in Cleaning & Sanitization, and ensure proper communications with internal and external customers and stakeholders.
  • Responsible for the health and safety of all personnel in areas of ownership, ensuring safety precautions are followed and safety hazards (including ergonomic risk) are reported and resolved in a timely manner.
  • Will be willing to become certified as a safety event first responder and take action in emergency situations.
  • Ensure all cleaning methods and materials are adequate, available, safe to use, and compliant with cGMP requirements.
  • Takes an active role in hiring, managing, coaching, and developing employees to ensure adherence to SOP's and cGMP.
  • Fosters a collaborative and psychologically safe team environment, leads daily huddles, resolves conflicts, and acts as a servant leader to meet the day-to-day needs of the staff.
  • Drives continuous improvement initiatives, 5S, and standard work to improve safety, cost, and effectiveness.
  • Is a role model for Quality/Right first time/Patient-focused culture by providing direct training, guidance, and problem-solving as necessary.
  • Monitors daily work coordination and distribution to maintain schedule adherence and cycle time.
  • Builds trust relationships and productive partnerships with cross-functional department teams, including QA, Sterility Assurance, and Microbiology.
  • Acts as a consultant to project teams to ensure impact to cleaning operations is considered.
  • Supports compliance audits and deviation investigations. May own actions based on audit or deviation findings.
  • This role is responsible for a team that works Night shift hours, 2x12 hour shifts, 7 days per week. Must be willing to work on site, with flexible hours but mainly on a swing shift schedule (~2pm-10pm) Monday through Friday.
  • This role is supported by shift leads but does require occasional on-call duty on weekends in instances of illness, emergency, or planned time off.
Requirements
  • 5+ years of experience in pharma/GMP environment, preferably in a direct manufacturing setting.
  • Minimum 1-2 years of leadership experience with demonstrated examples of leading and directing a team.
  • Well-versed in GMP manufacturing requirements, including good documentation practices, ALCOA+ principles, and sterility best practices.
  • Associate's or Bachelor's degree in a related field is preferred.
  • Minimum of high school diploma and/or equivalent combination of education and experience is required.
What We Offer

Bristol Myers Squibb offers a competitive salary and benefits package, including medical, pharmacy, dental, and vision care, as well as a 401(k) plan and other benefits. We also offer opportunities for professional growth and development, including training and education programs.

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