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Medical Writer
We are seeking an experienced Medical Writer with a strong background in Health Economics & Outcomes Research (HEOR), Health Policy, and Market Access communications to support the development of high-quality scientific and technical deliverables. The successful candidate will have experience working within the pharmaceutical, biotechnology, or hea...
Software Quality engineer
Software Validation Engineer (Contract) | Galway | 12 MonthsA leading medical device manufacturer is seeking an experienced Software Validation Engineer to support manufacturing and quality systems within a highly regulated environment. This is an excellent opportunity to join a major organisation and play a key role in ensuring critical equipment ...
Injection Equipment Engineer
Contract Injection Equipment Engineer (Freelance) Location: Lyon area, FranceContract Length: 12 monthsWorking Pattern: 40 hours per week - on-site Start Date: ASAP Overview A leading international manufacturer within a highly regulated industry is seeking an experienced Injection Equipment Engineer to support industrialisation and capital equipmen...
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Senior Process Engineer (6 months)
Senior Process EngineerLocation: Clermont-Ferrand, France Contract: Freelance Contractor Duration: 6 Months Language: French Preferred OverviewWe are seeking an experienced Senior Process Engineer to support a key manufacturing project near Clermont-Ferrand. The successful candidate will play a critical role in ensuring equipment, systems, document...
CQV Consultant
CQV Consultant (Contract)Location: Lyon Region, France (On-site) Contract Length: 12 Months Industry: Pharmaceuticals Start Date: ASAPThe OpportunityWe are supporting a leading pharmaceutical manufacturing site undergoing a significant capital investment and expansion programme. As part of this project, we are seeking an experienced CQV Consultant ...
Process Engineer
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...