Senior Cell Therapy Manufacturing Associate

Bristol Myers Squibb

Leiden

On-site

EUR 60,000 - 90,000

Full time

14 days+

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Job summary

Bristol Myers Squibb Netherlands is seeking an Associate III Manufacturing, Cell Therapy to support routine manufacturing operations within a GMP environment. You will work with a team to ensure safety, quality and compliance.

Responsibilities include executing SOPs and maintaining batch records, training operators, and supporting the Leiden facility as part of a fast-paced European cell therapy program. The role offers growth within a leading biopharma environment.

Qualifications

  • Associate or bachelor’s degree in related field preferred.
  • High school diploma or equivalent required.
  • 3+ years of cGMP cell therapy manufacturing experience.
  • Strong knowledge of GMP and FDA guidance applicable to biologics.
  • Excellent communication and teamwork skills.

Responsibilities

  • Execute operations as outlined in SOPs and batch records.
  • Perform tasks in a manner consistent with safety policies, SOPs, quality systems and GMP requirements.
  • Complete training assignments and train for proficiency in process systems.
  • Work within a controlled cleanroom environment and perform aseptic processing.
  • Complete documentation required by controlled documents and batch records.
  • Demonstrate strong practical and theoretical knowledge in their work.
  • Represent department in cross-functional collaborations and train others on SOPs.

Education

Associate / Bachelor’s degree in related field
High school diploma or equivalent

Job description

Bristol Myers Squibb Netherlands is seeking an Associate III Manufacturing, Cell Therapy to support routine manufacturing operations within a GMP environment. You will work with a team to ensure safety, quality and compliance.

Responsibilities include executing SOPs and maintaining batch records, training operators, and supporting the Leiden facility as part of a fast-paced European cell therapy program. The role offers growth within a leading biopharma environment.

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