Clinical Manufacturing Supply Quality Lead

What you'll do

• Safeguard the quality and release of clinical manufacturing and supply activities
• Define quality oversight for production, packaging, storage and distribution
• Review deviations, changes and validations across the clinical supply chain
• Review and maintain quality agreements with internal and external partners
• Guide partners through audits and escalations and make sure studies are supplied on time
• Translate regulations into practical controls and risk-based decisions

What you bring

• You hold a master's degree in pharmacy, life sciences or engineering
• You have hands-on GMP and GDP experience in a pharmaceutical environment
• You have experience with clinical supply, manufacturing quality or external partner oversight
• You are decisive and base your decisions on risk
• You collaborate easily in an international context

What you get

• You get a cross-functional quality role between production, supply and external partners
• You can work in a hybrid way in this role
• You work with an international scope and in international collaboration
• You receive a competitive pay and benefits package in line with the pharma sector
• You are hired directly on a permanent, full-time contract

How your application works

1. Introduction. We call you as soon as possible for a short introduction.
2. Interview at the client. A good fit? We put you forward and plan the interview together.
3. Offer and start. We guide you through to the signature, and beyond.