Cell Therapy Manufacturing Lead — GMP & Operations

Bristol Myers Squibb EU Policy; Leiden; On-site; EUR 90,000 - 120,000; Full time

Job summary

Bristol Myers Squibb Netherlands is seeking a Technical Lead Manufacturing for cell therapy to drive routine manufacturing operations in a GMP environment. You will support cell therapy programs, ensure safety, quality, and compliance, and collaborate across QA, QC, IT, and manufacturing teams in Leiden.

The role requires hands-on leadership, strong problem-solving, and the ability to guide cross-functional teams in a fast-paced biopharma setting while maintaining cGMP standards and achieving

Qualifications

• Bachelor's or equivalent in a related field preferred.
• MBO 3/4 in science-related field or equivalent experience.
• Extensive knowledge of cGMP cell therapy manufacturing is highly desired.

Responsibilities

• Execute SOPs and batch records.
• Lead frontline support team across multiple departments.
• Own deviations and lead investigations/CAPA development.
• Lead investigations (medium/complex) for technical, compliance and EHSS.
• Train GMP operations staff and manage GMP documentation.

Skills

Leadership

GMP knowledge

Education

Bachelor's degree in related field

MBO 3/4 in science related field

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 in a GMP environment. You will support cell therapy programs, ensure safety, quality, and compliance, and collaborate across QA, QC, IT, and manufacturing teams in Leiden.

The role requires hands-on leadership, strong problem-solving, and the ability to guide cross-functional teams in a fast-paced biopharma setting while maintaining cGMP standards and achieving