Are you a QP who wants more than just batch release? An environment where quality isn't a department but a mindset — and where your signature genuinely means something?

You'll be joining an internationally oriented biopharmaceutical production organisation in Amsterdam, specialising in GMP-compliant production of therapeutic proteins, vaccines and live microbials. A growing organisation where quality assurance is at the heart of everything — and where you, as QP, hold a pivotal role.

What will you do?

• Release investigational and commercial medicinal products, raw materials, APIs and finished products in accordance with applicable legislation and Marketing Authorisations
• Maintain quality oversight across all operational activities and act as the central point of contact for deviations, CAPAs and change controls
• Critically review investigations, interpret results and draw conclusions on product and facility impact
• Manage the pharmaceutical quality system and report KPIs, trends and deviations to management in a timely manner
• Represent the organisation during regulatory inspections and handle all associated correspondence and administration

What do you bring?

• University degree; qualified as QP in accordance with EU Directive 2001/83/EC, Eudralex Volume 4 Annexes 13 & 16
• Minimum 5 years of relevant (managerial) experience as a Qualified Person in the (bio)pharmaceutical industry
• Strong ability to maintain compliance without losing sight of operational continuity
• Excellent communication skills in English; able to translate complex quality matters into clear language
• Based in the Netherlands with a valid work permit

What do we offer?

A direct employment contract with our client — a professional, internationally oriented life sciences organisation in Amsterdam with an informal culture and a serious growth ambition. An attractive salary and a complete package of secondary benefits.

Does this sound like you? Apply now. If you're a match, we'll be in touch within 3 working days.

Please note: to be eligible for this position you must be based in the Netherlands and hold a valid work permit.