Qualified Person

Qualified Person (QP) - Netherlands

Shape quality. Lead excellence. Make an impact on global health.

• Are you a Qualified Person who thrives on responsibility, precision, and purpose?
• Do you take pride in knowing that your decisions directly ensure the safety, efficacy, and quality of medicines reaching patients across Europe and beyond?

If that sounds like you - this could be your next great opportunity.

We're looking for an experienced Qualified Person (QP) to take a leading role in the batch release and certification of commercial and clinical products for Europe . You'll be the cornerstone of quality assurance, ensuring that every product meets the highest global standards.

This is your chance to shape quality culture , lead a talented team , and influence the ambitious global growth of a dynamic, forward-thinking pharmaceutical organisation.

Your Impact

As a Qualified Person, you'll be responsible for ensuring the timely release and certification of both Investigational Medicinal Products (IMPs) and branded pharmaceuticals , in accordance with EU regulations (Annex 13 & 16, EudraLex Vol. 4).

You'll also provide leadership and oversight to a team of QPs , fostering a culture of excellence, collaboration, and continuous improvement within the Quality function. This is a strategic position where your expertise will directly influence the organisation's ambitious global growth plans - supporting an expansive and rapidly growing product pipeline that is propelling the company toward becoming one of the world's leading biopharmaceutical innovators .

Your key responsibilities will include:

• Certifying and releasing commercial and clinical batches in compliance with marketing authorizations and IMPDs
• Providing leadership, guidance, and oversight to the Qualified Person team
• Reviewing deviations, change controls, CAPAs, and transport conditions
• Supporting quality systems and inspection readiness for audits
• Advising on GxP requirements and quality strategy for clinical trials in Europe and beyond
• Partnering with cross-functional and global teams to drive continuous improvement

What You Bring

• Master's degree (or equivalent) in Pharmacy, Chemistry, or a related scientific field
• Officially recognized Qualified Person (QP) status
• At least 3 years of experience in pharmaceutical QA or QC roles (e.g. batch release, manufacturing QA)
• At least 2 years of experience in clinical operations or quality assurance for clinical trials in Europe
• Strong understanding of EU GMP, GDP, and GCP guidelines
• A proactive mindset, strong collaboration skills, and the ability to manage multiple priorities
• Experience in batch certification and team leadership will be strong assets.

What You'll Enjoy

• Flexible working arrangements to support your work-life balance
• 25 vacation days + your birthday off
• Comprehensive health insurance
• Professional development and growth opportunities
• A diverse, international working environment where your expertise truly makes a difference

Why Join Us?

This is more than a compliance role - it's a mission-critical leadership position in ensuring the safety and quality of medicines that reach patients across the world. You'll join a supportive, expert team that values precision, integrity, and innovation - right here in the Netherlands.

If you're ready to take ownership of quality at a global scale and help shape the future of pharmaceuticals, I'd love to hear from you .

Apply now and bring your expertise to where it matters most - improving lives through quality.