Part of Phaidon International
Part of Phaidon International
Showing 23 results
Sort by:
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...
Location: Lyon, France (Hybrid) Contract Length: 12 Months Start Date: Mid-October 2026 Engagement: Freelance We're supporting an established medical technology organisation developing innovative drug delivery and combination products. They are seeking an experienced Regulatory Affairs & Quality Consultant to lead key regulatory and quality initia...
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...
Take the first step toward your next opportunity - submit your resume and get started today.
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...
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...