Project Manager Qualification and Validation

Project Manager Qualification & Validation

Location: Hybrid
Type: Full-time

QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Qualification & Validation.

What’s in it for you?

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices

Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.

Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.

A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.

What you’ll be doing

As a Project Manager Qualification & Validation, you will be responsible for the planning, execution, and delivery of qualification and validation projects within life sciences.

• Lead qualification & validation projects within pharmaceutical, ATMP, and medical device industries.


• Develop and manage project plans, including scope, timeline, resources, and budget.


• Act as the primary point of contact for clients, ensuring alignment on project goals and expectations.


• Collaborate with internal departments (Sales, HR, Division Head) to support business development and resource planning.


• Organize and lead Steering Committees (SteerCo) to report on project progress, risks, and mitigation strategies.


• Ensure compliance with GMP, FDA, EMA, and other relevant regulatory requirements.


• Oversee validation activities including IQ/OQ/PQ for equipment, cleanrooms, utilities, HVAC systems, and processes.


• Support and guide validation specialists, providing coaching and training when necessary.


• Represent QbD Group during internal and external audits.

What you bring

• BSc/MSc degree in Life Science & Technology, Exact Science, Engineering, or a related field.


• At least 10 years of experience in Commissioning & Qualification (C&Q) within life sciences.


• You have a good understanding of Annex 1 guidelines for validation purpose.


• Fluent in Dutch and English.


• Strong project management skills, with experience managing multiple stakeholders.


• Excellent communication and leadership skills, capable of managing client relationships.


• Problem-solving mindset with a proactive and detail-oriented approach.


• Ability to work independently and as part of a team.

Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

• You’re resilient and tackle challenges with a positive mindset


• You’re curious and always up for learning something new


• You have a no non-sense approach honest, clear, respectful


• You’re innovative and bring ideas, not just opinions


• And above all, you’re serious about your work, but not too serious about yourself

✨ About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.

Interested? Let’s talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family