Senior Cell Therapy Manufacturing Leader

Bristol-Myers Squibb

Netherlands

Remote

EUR 110,000 - 150,000

Full time

14 days+
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Job summary

Bristol Myers Squibb Netherlands seeks a Senior Manager, Manufacturing, Cell Therapy to lead a team responsible for cell therapy manufacturing operations at the Leiden facility.

You will drive KPIs, ensure cGMP compliance, and coordinate cross-functional teams across QC, W&S, F&E, MFG to deliver safe, effective therapies for patients while advancing process improvements in a high-throughput environment.

Qualifications

  • 10+ years of experience in cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.
  • Minimum of 5+ years leading a team.
  • Cell therapy manufacturing experience preferred.
  • Leading cross-functional teams in a dynamic, high throughput environment.

Responsibilities

  • Establish department goals, track KPIs, and drive continuous improvement.
  • Head Emergency Response teams across multiple departments during emergencies and drills.
  • Authorized to order evacuation of the building and stop operations.
  • First point of contact in case of accidents and emergencies.
  • Own manufacturing unit operations, including equipment ownership, data analytics, procedures, MES recipes, and training content.
  • Lead resource scheduling in a matrix organization; design and operate manufacturing systems compliant with cGMP.
  • Ensure schedules for people, facility, equipment, materials, and documents meet capacity/throughput needs.
  • Identify and mitigate risks that could impact safe, effective therapies.
  • Champion inspection readiness efforts.
  • Establish team policies, structure, shift structure, and career ladders.

Skills

cGMP
Cell therapy
Bioprocessing
Leadership

Job description

Bristol Myers Squibb Netherlands seeks a Senior Manager, Manufacturing, Cell Therapy to lead a team responsible for cell therapy manufacturing operations at the Leiden facility.

You will drive KPIs, ensure cGMP compliance, and coordinate cross-functional teams across QC, W&S, F&E, MFG to deliver safe, effective therapies for patients while advancing process improvements in a high-throughput environment.

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