Responsible Person (RP)

Responsible Person (RP) Location : Hybrid, Utrecht Area, NL Type : Full-time Are you the vigilant, detail-driven professional who ensures that medicines not only get to patients — but get there safely, compliantly, and with confidence? We’re looking for a Responsible Person (RP) who knows that quality is more than a checkbox — it’s a promise. In this key role, you’ll be the cornerstone of GDP compliance, acting as the link between regulation, responsibility, and real-world patient impact. If you thrive in high-stakes environments, have a deep understanding of pharmaceutical distribution, and are ready to take ownership of quality — we’d love to meet you. 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 Take full ownership of ensuring GDP compliance throughout the supply chain — from product receipt to distribution — because quality is not negotiable Act as a trusted partner to internal teams, suppliers, and authorities, building strong, transparent relationships based on shared responsibility Oversee the implementation and continuous improvement of quality systems with a positive, hands-on approach Review and approve quality-related documentation (SOPs, deviations, CAPAs) with care, accuracy, and a mindset of continuous improvement Lead audits and inspections with confidence and clarity, representing the company and its values with professionalism Ensure that all personnel involved in GDP activities are trained and supported — success is something we build together Go the extra mile in monitoring and maintaining the quality of storage, transportation, and handling conditions Keep oversight of supplier qualification processes , ensuring partners meet our high standards and share our commitment to patient safety Stay ahead of changes in regulations and proactively adapt systems and processes — turning compliance into a strategic advantage Promote a culture of quality and accountability , helping others understand that doing the right thing is not a burden, but a shared goal What you bring You hold a Master's degree in pharmacy , medicine , chemistry , biology , or another relevant life sciences or technical field You have 1-3 year's work experience in a GDP environment You possess registration as Responsible Person with the Dutch MOH is preferred You have a solid understanding of quality systems , regulatory frameworks, and the principles that drive true quality assurance — not just on paper, but in practice You bring hands-on experience with quality assurance in operational environments , and you know how to assess, improve, and elevate processes that matter You’re comfortable working across disciplines like logistics, materials management, production, engineering, IT, quality control, and compliance — and you know how to connect the dots You think strategically without losing sight of the details — combining a sharp analytical mindset with a strong helicopter view to keep the bigger picture in focus 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.

Location: Utrecht area, NL

Posted Date: 7/30/2025