Part of Phaidon International
Part of Phaidon International
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Location: Southern France (exact site location to be discussed)Contract: 3-6 months (extension potential)Working Pattern: Primarily onsiteLanguages: Fluent French requiredOverviewWe are currently seeking experienced GMP Database & Data Migration Consultants to support a major pharmaceutical manufacturing modernization programme. The successful cons...
Key ResponsibilitiesSupport and execute process and technology transfer activities for sterile drug products.Prepare, review, and author GMP-compliant technical documentation and transfer packages.Evaluate manufacturing processes, equipment suitability, process performance data, and facility readiness.Review deviations, investigations, CAPAs, proce...
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...
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We are seeking an experienced Medical Monitor to support a global Phase III clinical trial in Leber Hereditary Optic Neuropathy (LHON). This is a part-time contract role (0.4 FTE) requiring an experienced physician with a strong background in rare diseases, ophthalmology, and late-phase clinical development.The Medical Monitor will provide ongoing ...
We are supporting a leading medical device manufacturer seeking an experienced Validation Engineer to support equipment qualification and manufacturing validation activities across a regulated production environment.This role will play a key part in delivering validation projects for new and existing manufacturing equipment, ensuring compliance wit...
Freelance Injection Equipment EngineerAssignment OverviewOur client is seeking an experienced Freelance Injection Equipment Engineer to provide specialist engineering support across injection moulding equipment projects within a regulated manufacturing environment. The consultant will work alongside relevant project stakeholders to support the intr...