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...
OverviewWe are seeking experienced quality professionals to support a major pharmaceutical manufacturing client in Greenville, North Carolina. This engagement focuses on strengthening quality oversight, manufacturing compliance, remediation activities, and inspection readiness efforts within a regulated GMP environment.Consultants will join an esta...
Quality Director/Head of QualityAs the site's Leadership Team member, the QA Director will lead and direct the daily activities of Quality Assurance supporting the Company's analytical operations. Develop, implement, maintain and improve upon the cGMP compliant systems in alignment with the company and corporate quality strategies and objectives. C...
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Location: Ghent, Belgium (On-site) Contract Type: Consultant / Freelance Duration: 6 Months Department: Quality Assurance Industry: Pharmaceutical Manufacturing Languages Required: Fluent Dutch and EnglishOverviewOur client, a leading pharmaceutical manufacturer based in Ghent, Belgium, is seeking an experienced QA C&Q Engineer to support the ongoi...
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...
OverviewWe are seeking an experienced pharmaceutical professional with direct plasma fractionation manufacturing experience to support ongoing operations and project activities at a pharmaceutical site in Strasbourg.The role is open to candidates from a range of backgrounds, including Process Engineering, CQV, Manufacturing, Production, Validation...