CSV Engineer - Geel, Flemish Region
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Join an exciting environment where your expertise can play a crucial role in ensuring compliance and quality in the pharmaceutical sector. We are looking for a dedicated professional to drive the validation processes for critical computerized systems, ensuring they meet stringent ...
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We are looking for a dedicated professional to drive the validation processes for critical computerized systems, · You develop and implement URS SIA DQ IQ OQ PQ RV TM activities. · You generate validation documentation including protocols and reports ensuring compliance with cGMP ...
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This position may be a great fit for you if you are detail-oriented, technically adept, and thrive in a compliance-focused environment. · ...
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Ensure digital systems stay audit‑ready as the Validation Engineer powering compliance in a leading pharma hub. · R&D Partners is seeking a Validation Engineer CSV to join a leading pharmaceutical company in Geel, Belgium. This role focuses on ensuring compliance with cGMP standa ...
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Ensure digital systems stay audit‑ready as the Validation Engineer powering compliance in a leading pharma hub. · R&D Partners is seeking a Validation Engineer CSV to join a leading pharmaceutical company in Geel, Belgium. This role focuses on ensuring compliance with cGMP standa ...
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We are seeking a Validation Engineer with hands-on experience in validating cGMP-critical computerized systems. · ...
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Onze klant, een toonaangevend farmaceutisch productiebedrijf, zoekt een gemotiveerde Junior CSV Engineer voor hun site in Geel. De rol richt zich op Computer System Validation (CSV) binnen een streng gereguleerde GMP-omgeving waar kwaliteit en patiëntveiligheid centraal staan. · ...
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Onze klant zoekt een gemotiveerde Junior CSV Engineer. · Je voert Computer System Validation (CSV) activiteiten uit ter ondersteuning van het validatieteam. · ...
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:Key Accountabilities: · Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical computerized systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. ...
3 dagen geleden
: · Key Accountabilities: · Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical computerized systems to demonstrate compliance to cGMP-, User- and Regulatory requiremen ...
3 dagen geleden
Onze klant zoekt een gemotiveerde Junior CSV Engineer voor hun site. · De rol richt zich op Computer System Validation (CSV) binnen een streng gereguleerde GMP-omgeving. · Patiëntveiligheid staat centraal. · ...
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I'm currently partnering with a global industry-leading pharmaceutical company that is expanding its manufacturing operations. · ...
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We are looking for a Quality Assurance Computer System Validation Engineer · We as QA CSV group belong to the Quality organization of Johnson & Johnson Innovative Medicine Supply Chain (IMSC) and are responsible to ensure the quality and compliance of different systems on the J& ...
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Join a cutting-edge team dedicated to ensuring the highest standards in computerized systems validation (CSV) within the regulatory framework. · ...
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The Advanced Therapy Quality team from Johnson & Johnson Innovative Medicine is recruiting a QA CSV engineer for the CAR-T Hub in Europe. The position will be based in Ghent Belgium. · ...
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The Advanced Therapy Quality team from Johnson & Johnson Innovative Medicine is recruiting a QA CSV engineer for the CAR-T Hub in Europe. The position will be based in Ghent Belgium. · To assure that all Computer Systems Validation related regulatory requirements are fulfilled d ...
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· General information · Publication date · /08/2025 · Category · OPERATIONS - ENGINEERING/PRODUCTION · Job title · CSV Engineer - Life Sciences - M/V/X · Contract · Permanent contract · Job description · Functieomschrijving: CSV Engineer · Locatie: Beerse · Overzicht: · Wij op z ...
2 dagen geleden
Jouw Rol · Onze klant, een toonaangevende speler binnen de farmaceutische productie, versterkt zijn organisatie met een Junior CSV Engineer. In deze rol werk je binnen een hooggereguleerde GMP‑omgeving, waar kwaliteit, betrouwbaarheid en continue verbetering centraal staan. Je ma ...
4 dagen geleden
We are seeking a skilled and motivated Validation Engineer to join our team, · supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment.Develop, implement, and execute User Requirement Specifications (URS), System Impact Assessment (SIA ...
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We are seeking a skilled and motivated Validation Engineer to join our team supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment. · Minimum 3 years of experience in a pharmaceutical or life sciences environment within a GMP-regulate ...
3 weken geleden