- This role focuses on qualification activities for manufacturing equipment or facility & utility systems, depending on your background.
- Equipment Qualification: Manufacturing equipment used in pharmaceutical/chemical environments, Automation or production systems, Equipment-related risk assessments, FAT/SAT, commissioning, IQ/OQ/PQ
- Facility & Utility Qualification: HVAC, purified water clean steam building systems Facility infrastructure or clean utility systems Utility environmental qualification processes
- Support qualification activities across the full lifecycle concept → retirement
- Review and approve
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We zijn momenteel op zoek naar een QA specialist voor productie plant · In deze functie ben je verantwoordelijk voor quality ondersteuning van de operations activiteiten van een multiproduct faciliteit. · Opstellen en reviewen van Quality documentation in kader van project (Proj ...
Geel1 maand geleden
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We zijn momenteel op zoek naar een QA specialist voor productie plant 1. · ...
Geel, Flemish Region1 maand geleden
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Supports QA Engineering in ensuring qualification-related regulatory requirements are met throughout manufacturing systems lifecycle. · ...
Geel2 weken geleden
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Contract until: · 31/12/2026 · Experience: · 4–6 years · Languages: · English & Dutch · We are hiring a · QA Qualification Contractor · in Geel. This role focuses on qualification activities for · either manufacturing equipment · or · facility & utility systems · , depending on y ...
Geel, Flemish Region1 week geleden
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Contract until: 31/12/2026 · Experience: 4–6 years · Languages: English & Dutch · We are hiring a QA Qualification Contractor in Geel. This role focuses on qualification activities for either manufacturing equipment or facility & utility systems, depending on your background. · W ...
Geel1 week geleden
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A specialised organisation active in nuclear medicine and radiopharmaceutical manufacturing is strengthening its Quality function to support ongoing production and scale-up activities. · The company operates in a highly regulated environment and plays a critical role in supplying ...
Mol1 maand geleden
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Randstad Professional Life Sciences in Vlaanderen zoekt een Quality Assurance Specialist/Batch Record Reviewer. In deze rol speel je een cruciale rol in de kwaliteitsborging van klinische studiemedicatie. · ...
Beerse1 maand geleden
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Randstad Professional Life Sciences zoekt naar QA specialist - supplier quality. · ...
Antwerp1 maand geleden
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Randstad Professional Life Sciences zoekt naar een QA Specialist - Supplier Quality. · Ben jij een kwaliteitsgerichte professional met een passie voor externe partnerships?Kwaliteitstoezicht: · Compliance & Risicobeheer: · Operationele QA: · ...
Antwerp Metropolitan Area1 maand geleden
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Quality Assurance - Qualified Person (QP) - Investigational Medicinal Products - IMP · Location: Beerse, Belgium · Duration of the contract: Until 31st December 2026 · Hours per week: 40 hours (hybrid working 3 days onsite, 2 days home office) · Essential: Qualified Person (QP) - ...
Beerse 38.000 € - 65.000 € (EUR) per jaar1 week geleden
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We are seeking an experienced freelance QA professional who can step into a regulated manufacturing environment and add immediate value. · ...
Antwerp1 maand geleden
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We are seeking an experienced QA associate to join our quality team.The ideal candidate will have a strong background in quality assurance and a deep understanding of industry regulations. · ...
Antwerp1 maand geleden
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We are seeking an experienced QA associate to join our quality team. · The ideal candidate will have a strong background in quality assurance, · a keen eye for detail, · and a deep understanding of industry regulations.Batch record review · Release of incoming raw materials · Sup ...
Antwerp, Flemish Region1 maand geleden
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As a Sterility Assurance Quality Specialist at Capgemini Engineering, · a world-leading engineering services company, · You will play a crucial role in ensuring the highest standards of quality and compliance in pharmaceutical manufacturing processes. · ...
Machelen1 maand geleden
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As a Sterility Assurance Quality Specialist you will play a crucial role in ensuring the highest standards of quality and compliance in pharmaceutical manufacturing processes. · ...
Machelen Voltijd1 maand geleden
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Senior Freelance Quality Assurance Specialist – Food Manufacturing · Belgium (Flanders & Wallonia) | On-site with flexibility depending on project · 6–12 Month Contract | High Probability of Extension · Freelance Engagement Only (Independent / Consultancy Structure Required) · Th ...
Antwerp1 dag geleden
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Sterility assurance quality specialist plays a crucial role in ensuring high standards of quality and compliance in pharmaceutical manufacturing processes. · ...
Diegem1 maand geleden
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We are seeking a Material Qualification Specialist to support Material Qualification and Product Development activities within the Therapeutics Development & Supply organization. · This hybrid role offers 50% onsite/remote working arrangements. · ...
Machelen1 maand geleden
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Ensure the highest standards of quality and compliance in pharmaceutical manufacturing processes as a Sterility Assurance Quality Specialist at Capgemini Engineering. · Driving and executing continuous improvement projects and remediation plans related to sterility assurance. · ...
Diegem, Flemish Region1 maand geleden
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Support Material Qualification and Product Development activities within the Therapeutics Development & Supply organization. · ...
Machelen Voltijd1 maand geleden
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Sterility Assurance Quality Specialist | Life Sciences. As a Material Qualification Specialist in our Life Sciences division, you will support Material Qualification and Product Development activities within the Therapeutics Development & Supply organization. · ...
Diegem1 maand geleden
Senior Quality Assurance Specialist - Geel - Allegis Group
Beschrijving
Senior Quality Assurance Specialist
Join Allegis Group in Geel, BE as a QA Qualification Contractor and contribute to high-impact qualification work in a leading pharmaceutical environment.
About the Role:
The ideal candidate will have 4–6 years of relevant industry experience (pharma or chemical) with strong knowledge of cGMP and qualification/validation principles. Fluency in English & Dutch is required along with excellent communication skills.
Your Background:
We welcome candidates with experience in either of the following areas:
You'll Do:
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Quality Assurance Specialist
Alleen voor geregistreerde leden Geel
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Quality Assurance Specialist
Alleen voor geregistreerde leden Geel, Flemish Region
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Quality Assurance Specialist
Alleen voor geregistreerde leden Geel
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Senior Quality Assurance Specialist
Alleen voor geregistreerde leden Geel, Flemish Region
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Senior Quality Assurance Specialist
Alleen voor geregistreerde leden Geel
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Quality Assurance Specialist
Alleen voor geregistreerde leden Mol
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Quality Assurance Specialist
Alleen voor geregistreerde leden Beerse
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Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp
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Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp Metropolitan Area
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Quality Assurance Specialist
Alleen voor geregistreerde leden Beerse
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Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp
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Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp
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Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp, Flemish Region
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Sterility Assurance Quality Specialist
Alleen voor geregistreerde leden Machelen
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Sterility Assurance Quality Specialist
Voltijd Alleen voor geregistreerde leden Machelen
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Senior Quality Assurance Specialist
Alleen voor geregistreerde leden Antwerp
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Sterility Assurance Quality Specialist
Alleen voor geregistreerde leden Diegem
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Sterility Assurance Quality Specialist
Alleen voor geregistreerde leden Machelen
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Sterility Assurance Quality Specialist
Alleen voor geregistreerde leden Diegem, Flemish Region
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Sterility Assurance Quality Specialist
Voltijd Alleen voor geregistreerde leden Machelen
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Sterility Assurance Quality Specialist
Alleen voor geregistreerde leden Diegem