Part of Phaidon International
Part of Phaidon International
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OverviewWe are seeking an experienced Data Integrity Project Manager to lead the deployment and implementation of a large-scale data integrity programme across multiple pharmaceutical manufacturing sites. The successful candidate will act as the primary interface between manufacturing sites, system vendors, engineering partners, and project stakeho...
Location: Geel, BelgiumContract duration: 12 months + OverviewAn exciting opportunity is available for an experienced Senior Quality Engineer specialising in Cleaning Validation to join a leading pharmaceutical manufacturing site in Geel, Belgium. The role supports quality oversight activities across cleaning validation programmes, ensuring complia...
Quality Assurance Specialist Duration: 12 months (with extension opportunity)Hours: Full-time (hybrid)Location: Leuven, BelgiumEngagement: Freelance Key ResponsibilitiesMaintain and update Risk Management Files in line with ISO 14971 requirementsPerform risk assessments, hazard analyses, and benefit-risk evaluations for new and existing productsAss...
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Senior Quality Assurance Consultant (GMP Manufacturing Operations)We are currently supporting a major pharmaceutical manufacturing organisation on a high-profile quality and compliance improvement programme and are seeking experienced Senior Quality Assurance professionals to join on a contract basis.This opportunity is specifically aimed at indivi...
OverviewWe are seeking an experienced QA Qualification / Validation Engineer to join a highly regulated pharmaceutical manufacturing environment. This role provides Quality Assurance oversight for qualification, validation, commissioning, and lifecycle management activities related to manufacturing systems, process equipment, laboratory equipment, ...
Location: Belgium (Beerse / Ghent) Contract: Freelance Consultant Industry: Pharmaceutical & Biotechnology OverviewWe are supporting multiple strategic programmes within a global pharmaceutical environment and are looking to engage experienced QA-CSV, Digital Compliance and Computerised Systems Validation professionals.Opportunities are available a...