For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Position overview
ProPharma is currently supporting an international Pharmaceutical group as they require support for their GDP QA activities within the Netherlands and Belgium. This project is to be the acting Responsible Person and Quality Manager for the region; it will ideally commence in March and will run for at least 3-6 months while our client appoints a permanent individual. The role can be performed largely remotely; it requires 3 days a week support throughout and requires demonstrated skills working as an Responsible Person in Netherlands or Belgium.
In this position, you will act as the Responsible Person/Quality Manager to help ensure all regulations are met to continue to distribute our client’s products within the region. In addition, you will maintain an overview of the supply chain activities; review and approve change requests, deviation reports, CAPA’s as well as liaising with Regulatory authorities. You will also have the opportunity to provide strategic advice, support QA activities in general; support Technical Operations teams and prepare for any Healthcare authority inspections.
Qualifications
A University degree in Science/Engineering is required, preferably MSc in Pharmacy or similar.
Must be able to demonstrate thorough experience working as a Responsible Person within the Netherlands or Belgium (current experience would be highly preferred)
Thorough experience working in Quality Assurance with extensive skills working within GDP QA
Fluency in English and Dutch (or French) would be required
Currently based in the Netherlands or Belgium
Can perform the project to the required needs within the job description
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We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
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What We Do
ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science







