Cell Therapy Manufacturing Lead

Bristol Myers Squibb

Leiden

On-site

EUR 90,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Health insurance
On-site facilities

Job summary

Bristol Myers Squibb Netherlands is seeking a Technical Lead Manufacturing for Cell Therapy to drive routine manufacturing operations and ensure GMP compliance. You will lead a matrix frontline team across QA, QC, IT, MFG, and related groups, maintain schedules, own deviations, and mentor staff in GMP practices.

The role requires strong cross-functional collaboration, technical acumen, and a proactive approach to problem solving in a high-stakes manufacturing environment.

Qualifications

  • Associate or Bachelor's degree in a related field preferred.
  • MBO 3/4 in science or equivalent with manufacturing experience.
  • 4+ years in cGMP cell therapy manufacturing or related field.
  • Extensive knowledge of cGMP regulations and FDA guidance.

Responsibilities

  • Execute operations per SOPs and batch records.
  • Lead frontline support team across multiple departments.
  • Manage schedule adherence and communicate variances.
  • Own deviations and lead investigations/CAPA development.
  • Train GMP operations staff and ensure traceability of documentation.
  • Support daily unit operations and cross-functional collaboration.
  • Drive RFT execution and continuous process improvements.

Skills

GMP knowledge
Leadership
Problem solving
Team collaboration
Schedule adherence
Process optimization
Training & mentoring

Education

Associate or Bachelor's degree in a related field
MBO 3/4 in science or equivalent
4+ years cGMP cell therapy manufacturing experience

Tools

Word processing
Spreadsheets
Web-based applications

Job description

Bristol Myers Squibb Netherlands is seeking a Technical Lead Manufacturing for Cell Therapy to drive routine manufacturing operations and ensure GMP compliance. You will lead a matrix frontline team across QA, QC, IT, MFG, and related groups, maintain schedules, own deviations, and mentor staff in GMP practices.

The role requires strong cross-functional collaboration, technical acumen, and a proactive approach to problem solving in a high-stakes manufacturing environment.

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