Senior Associate Ii Manufacturing, Cell Therapy

Bristol Myers Squibb

Leiden, NL
Hybrid (50% onsite)
7+ years cgmp cell therapy manufacturing experience
Knowledge of good manufacturing practices (gmps)
Experience with standard operating procedures (sops)
Bristol Myers Squibb is seeking a Senior Associate II for its Cell Therapy Manufacturing team in Leiden, NL, where candidates will play a crucial role in supporting routine manufacturing operations. The ideal candidate should possess knowledge in Good Manufacturing Practices (GMP) and be an expert in complex manufacturing processes

Job Summary

  • This role involves driving novel cell therapy programs by supporting routine manufacturing operations at a state-of-the-art facility in Leiden, The Netherlands.
  • Candidates must demonstrate strong practical knowledge of cGMP regulations and serve as a subject matter expert on complex manufacturing unit operations.
  • The position offers the opportunity to join a high-achieving team focused on transforming patients' lives through personalized blood cancer treatments.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Associate II for its Cell Therapy Manufacturing team in Leiden, NL, where candidates will play a crucial role in supporting routine manufacturing operations. The ideal candidate should possess knowledge in Good Manufacturing Practices (GMP) and be an expert in complex manufacturing processes.

Skills & Requirements

Must-have

  • 7+ years cGMP cell therapy manufacturing experience
  • Knowledge of Good Manufacturing Practices (GMPs)
  • Experience with Standard Operating Procedures (SOPs)
  • Ability to work in controlled cleanroom environment
  • Proficiency in aseptic processing procedures

Nice-to-have

  • Peer-level floor leadership experience
  • Positive attitude and team culture building
  • Innovative problem-solving skills
  • Strong interpersonal and communication skills
  • Aptitude for engineering principles

Key Requirements

  • MBO 3 or 4 in science related field
  • 7+ years of cGMP cell therapy manufacturing experience
  • Extensive knowledge of FDA guidance for biologics
  • Demonstrated proficiency in computer tools

Work Rights

Not specified

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