Clinical Supply Chain Project Manager (GMP/Regulatory)

Warman O'Brien; Lelystad; On-site; EUR 70,000 - 90,000; Full time

Job summary

Warman O'Brien in the Netherlands is seeking a Clinical Supply Chain Project Manager to oversee a 12-month contract, with extension or potential permanent role. The successful candidate will coordinate cross-functional teams and ensure alignment with GMP and regulatory guidelines, to support clinical supply activities in Lelystad.

The role requires strong project management, external stakeholder engagement, and experience with packaging, labeling, and blinding processes in a GMP environment.

Qualifications

• Strong knowledge of the clinical supply chain.
• Project management experience.
• Managing external stakeholders.
• Knowledge and understanding of GMP and local/regional regulatory guidelines.
• Experience working in a GMP regulated environment.
• Packaging, labeling and blinding experience (randomized placebo experience is highly desired).

Skills

Clinical supply chain

Project management

Stakeholder management

GMP knowledge

Packaging & labeling

Blinding experience

Job description

Warman O'Brien in the Netherlands is seeking a Clinical Supply Chain Project Manager to oversee a 12-month contract, with extension or potential permanent role. The successful candidate will coordinate cross-functional teams and ensure alignment with GMP and regulatory guidelines, to support clinical supply activities in Lelystad.

The role requires strong project management, external stakeholder engagement, and experience with packaging, labeling, and blinding processes in a GMP environment.