Save Job Back to Search Job Description Summary Similar Jobs Added 17/08/2026Submit your CV to be the first in line for new opportunities that open this fallJoin a specialised network trusted by leading healthcare employersAbout Our ClientOur clients are established healthcare organisations operating across the medical devices and pharmaceutical sectors. These companies are actively strengthening their Quality and Regulatory Affairs teams to support growth, compliance, product launches, and market expansion within the Dutch and European markets.Job DescriptionAs a Quality or Regulatory professional, you will play a key role in ensuring compliance with industry regulations and maintaining the highest standards throughout the product lifecycle. Your experience will be matched with opportunities aligned to your seniority, expertise, and career ambitions.Ensure compliance with applicable regulations, standards, and quality requirementsSupport and maintain Quality Management Systems (QMS)Prepare, review, and manage regulatory submissions and technical documentationLead or support audits, inspections, CAPAs, and risk management activitiesCollaborate with cross-functional teams including R&D, Operations, Clinical, and Commercial functionsThe Successful ApplicantYou understand the regulatory landscape within the medical devices or pharmaceutical industry and have experience operating in a regulated environment. You are based in the Netherlands and are interested in exploring new opportunities for the coming months.Experience in a Quality or Regulatory Affairs role at Associate, Specialist, or Manager levelBackground within the medical devices and/or pharmaceutical industryKnowledge of industry-specific regulations and quality standards such as MDR, IVDR, ISO 13485, GMP, GDP, or related frameworksCurrently based in the Netherlands with professional experience in the Dutch marketBachelor's degree or higher in Life Sciences, Pharmacy, Biomedical Sciences, Engineering, Quality Management, or a related disciplineStrong stakeholder management, documentation, and communication skillsProfessional proficiency in English; Dutch is beneficial for some opportunitiesWhat's on OfferCompetitive salary packages aligned with experience and levelPerformance-based bonus opportunities and attractive benefitsAccess to vacancies that may not be publicly advertisedOpportunities within both international market leaders and innovative healthcare organisationsLong-term career development within Quality Assurance and Regulatory AffairsExposure to high-impact projects involving compliance, product registration, and quality improvement initiativesContactKaitlyn HalleranQuote job refJN-082026-7084632Job summarySectorHealthcare & Life SciencesSub SectorQuality & Regulatory AffairsIndustryHealthcare / Pharmaceutical Jobs by locationNetherlandsContract TypePermanentConsultantKaitlyn HalleranJob ReferenceJN-082026-7084632
