Study Manager, Biosafety Testing GMP Leader

Leiden Bio Science Park; Leiden; On-site; EUR 65,000 - 85,000; Full time

Benefits offered by this job

Competitive salary

Flexible working hours

25 days vacation (+7)

Job summary

Eurofins BioPharma Product Testing Leiden B.V. seeks a Study Manager to ensure high-quality study design, execution and documentation. You translate inquiries into robust protocols, prepare structured reports, interpret results and coordinate troubleshooting with the lab team.

You will guide analysts, communicate progress to customers in English, and support QA during audits, with a focus on GMP compliance and cross‑department collaboration.

Qualifications

• Master's degree in Life Sciences, Molecular Biology, or related field.
• Experience in a similar role, preferably in a lab or research environment.
• Familiarity with GMP guidelines.
• Experience with cell biology and/or molecular biology techniques.
• Excellent written and verbal communication in English; Dutch is a plus.
• Customer- and result-oriented team player who coordinates with QA, Marketing and Sales.

Responsibilities

• Translate customer inquiries into clear study protocols and prepare well-structured study reports.
• Design, execute, and document studies to the highest quality standards.
• Review and interpret test results, identify deviations, and coordinate troubleshooting.
• Collaborate with laboratory teams and provide scientific guidance and support.
• Communicate with customers on study progress and outcomes.
• Coordinate with QA and other departments; assist during audits from a scientific perspective.

Skills

Excellent English communication

Team player

Customer-oriented

Result-oriented

Coordination with QA/Marketing/Sales

Education

MSc in Life Sciences or Molecular Biology

Tools

Cell biology techniques

Molecular biology techniques

Job description

Eurofins BioPharma Product Testing Leiden B.V. seeks a Study Manager to ensure high-quality study design, execution and documentation. You translate inquiries into robust protocols, prepare structured reports, interpret results and coordinate troubleshooting with the lab team.

You will guide analysts, communicate progress to customers in English, and support QA during audits, with a focus on GMP compliance and cross‑department collaboration.