Job Opening
QA officer
Connect quality and patient safety in the Benelux within a committed family-owned pharmaceutical company
- Location: Weesp
Who are we?
Truvion Healthcare is a dynamic, independent family-owned company with over 50 years of experience in the pharmaceutical sector. From offices in the Benelux and the United Kingdom, they develop and deliver innovative medicines, care concepts, and services – always tailored to individual patient needs.
With a strong focus on gastroenterology and rheumatology, they work closely with healthcare professionals and pharmacists. The organization is inspired by the Vitruvian principle: the human at the center. At Truvion, you’ll work in a committed and informal work environment where your contribution matters – for the team and for the patient.
Offer
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A versatile QA role with broad responsibilities within GDP/GMP, focusing on the Benelux region;
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Working in a dynamic, close-knit team with short communication lines and a personal approach;
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Room for initiative, professional development, and a real impact on patient care;
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Opportunity to grow into a RP.
Position
As a QA Officer, you play a central role in safeguarding the quality of distribution processes. You manage and implement the GDP quality system and ensure compliance with all relevant laws and regulations. You develop, update, and implement procedures and provide internal training for colleagues. You also manage deviations, CAPAs, and Change Control plans.
As the delegate of the Responsible Person, you support the administrative release of products, the assessment of returned goods, and the preparation and supervision of inspections and internal and external audits. You also coordinate the handling of complaints and ensure accurate and up-to-date QA documentation.
In short: a versatile role in which you connect compliance, process optimization, and patient safety within a people-focused organization.
Profile
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Completed university or higher professional education (HBO) degree, preferably in pharmaceutical sciences;
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At least 3 years of experience in Quality Assurance within the pharmaceutical industry;
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Thorough knowledge of GDP/GMP regulations and experience with audits, CAPAs, and QMS;
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Analytical and practical approach, proactive, with an eye for detail;
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Excellent communication skills in Dutch and English (French is a plus).
Application
Interested? Send your resume and cover lettter, quoting reference number WS/25-207, to Dennis Uleman, info@derksenderks.nl.
For more information, please call, text or WhatsApp Dennis Uleman at +31 6 82 72 71 33.
An assessment may be part of the selectionprocess.