Part of Phaidon International
Part of Phaidon International
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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...
Location: BelgiumStart Date: ASAPContract Length: 12 months (freelance)Hours: Full-time - 5 days per weekWorking Arrangement: HybridI'm currently partnering with a global life sciences company providing technologies and services that support the development and manufacture of biopharmaceuticals and advanced therapies. I'm seeking a QA Specialist on...
Quality Validation & Documentation ConsultantLocation: Singapore (Onsite)Contract Length: 12 MonthsStart Date: ImmediateOur client is seeking an experienced Quality Validation & Documentation Consultant for a 12-month onsite contract in Singapore. This hands-on role will support validation and GMP quality activities within a regulated manufacturin...
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Responsible Person (RP) ConsultantLocation: London (Hybrid) Contract: Part-Time We are currently partnering with an established organisation operating within the Medical Device and Life Sciences sector that is seeking an experienced Responsible Person (RP) to provide specialist quality and compliance support on a contract basis.This is an excellent...
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...
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...