🔍 Responsible Person

📍 Location: Hybrid
🕓 Type: Full-time

We are looking for colleagues who are interested in taking up the role of Responsible Person (RP) for GDP-related activities within client projects.

This is an internal opportunity for consultants who meet the legal requirements to act as RP and who would like to support projects where an RP is required. The role does not need to be full-time and can be taken up on an ad hoc basis, depending on project needs and availability.

💡 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

• Act as Responsible Person (RP) in accordance with EU Good Distribution Practice (GDP) guidelines (2013/C 343/01).

• Ensure that medicinal products are handled, stored and distributed in compliance with GDP requirements.

• Ensure the quality management system related to distribution activities is implemented and maintained.

• Review and approve GDP-related documentation (e.g. deviations, CAPAs, change controls, procedures).

• Ensure personnel involved in distribution activities are appropriately trained.

• Support and participate in audits and inspections.

• Provide quality oversight for distribution and logistics activities.

💪 What you bring

To legally act as a Responsible Person (RP) under EU GDP requirements, candidates must meet the following criteria:

Education (as defined in EU GDP guidelines):

• A university degree (or equivalent qualification) in one of the following fields:

  • Pharmacy

  • Chemistry

  • Biology

  • Biochemistry

  • Pharmaceutical sciences

  • Medicine

  • or another relevant life sciences discipline

Experience:

• Practical experience in GDP or pharmaceutical quality systems, typically at least 1–2 years in activities related to pharmaceutical distribution or quality management.

• Good knowledge of EU GDP guidelines and pharmaceutical regulatory requirements.

• Experience with quality systems, audits or inspections is an advantage.

🫵 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.