🔍 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.
- 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