Regulatory Compliance Officer

Regulatory Compliance OfficerpbHartwig Medical Foundation /b /pbrControleer of u voldoet aan de vaardigheidseisen voor deze functie, evenals de bijbehorende ervaring, en solliciteer vervolgens met uw cv hieronder.brpWe seek an experienced Regulatory Compliance Officer to take ownership of IVD/MD compliance for our software products and data‑driven tools. You will join a small, dedicated team committed to delivering the best molecular diagnostics for patients with cancer. Your autonomy and expertise will directly impact our product lifecycle and regulatory strategy. /ppbMission /b: Contribute to improving care for patients with cancer by ensuring regulatory compliance and supporting evidence‑based decision making. /ppbKey Responsibilities /b: /pulliLead IVD/MD compliance for software products and tools, including the creation and maintenance of technical documentation for new products and version releases. /liliCoordinate and align the organization’s accreditation strategy and implementation plans with international quality requirements of our clients and product users. /liliCoordinate risk management processes and ensure general safety and performance requirements are translated into verifiable design criteria. /liliOversee post‑market surveillance (PMS), including Performance Evaluation Reports (PER), Periodic Safety Update Reports (PSUR), risk analysis updates, and reporting obligations to Competent Authorities and Notified Bodies. /liliServe as the main point of contact for regulatory authorities and Notified Bodies, and work closely with the Quality Manager to align regulatory requirements with QMS processes. /liliEducate colleagues on IVDR/MDR and ISO13485 requirements and advise management on regulatory strategy and compliance matters. /li /ulpbYour Profile /b: You are driven by solving complex problems and making an impact in fast‑paced environments. Proactive, solution‑oriented, and collaborative, you enjoy working with software developers and exploring data analytics in life sciences. /ppbYour Background Includes /b: /pulliDegree in life sciences, engineering, bioinformatics, or a related scientific field. /lili5+ years in regulatory affairs or quality management, including 2+ years in IVDR/MDR. /liliSolid understanding of IVDR/MDR regulations. /liliBasic knowledge of software products and development processes. /liliStrong communication skills in English (Dutch is a plus). /li /ulpbWhy us? /b /pulliMeaningful role (32–40 hours per week) in a mission‑driven, non‑profit organization. /liliCompetitive salary. /lili26 vacation days per year (full‑time). /liliHartwig contributes two‑thirds to your pension. /liliHybrid working environment, combining office presence with remote work. /lili€0.23 per kilometre for commuting. /liliGenerous office lunch on Tuesdays and Thursdays, Friday drinks and annual company events. /liliA dynamic, multidisciplinary team with an informal, open culture. /liliAccess to the Hartwig Academy for professional development, growth, and certification opportunities. /li /ulpbApply! /b If this role excites you, click the application button or send an email to with your CV and cover letter. The application process includes two interviews, a motivation assessment, and a reference check. /ppbAbout Us /b: Every day we work with one clear goal: to ensure that every patient with cancer receives the treatment best suited to their unique situation. We develop comprehensive DNA testing to help hospitals analyze tumors with precision and support clinicians in making informed treatment decisions. Our rich knowledge base on patients, tumors, and treatment outcomes drives breakthroughs for future care. We collaborate closely with hospitals, researchers, and partners across the Netherlands to lower barriers to personalized cancer care. xgiwjmb Join our multidisciplinary team of experts—including medical professionals, analysts, bioinformaticians, and software developers—to make a real impact on patient care. /ppLocation: Science Park 408, 1098 XH, Amsterdam, Netherlands /pbr