Part of Phaidon InternationalProperty 1 Bull Dark

You are viewing the United Arab Emirates [EN] site. to view your country site linked to your browser settings

Jobs in Lyon, Auvergne Rhne Alpes

Get job alerts

Showing 5 results

Sort by:

Injection Equipment Engineer
LyonNegotiable

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...

CQV Consultant
LyonNegotiable

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 ...

Data Integrity Lead
LyonNegotiable

Data Integrity & CSV Program ManagerLocation: Lyon, France Start: Approximately 1-2 months Duration: 12 months Language: Fluent French requiredRole OverviewWe are seeking an experienced Data Integrity & CSV Program Manager to lead a large-scale Data Integrity programme within a pharmaceutical manufacturing environment.The programme will involve the...

Elevate your career

Take the first step toward your next opportunity - submit your CV and get started today.

Register CV
Selby Jennings Start Your Career In Recruitment
Regulatory Affairs & Quality Consultant
LyonNegotiable

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...

Process Engineer
LyonNegotiable

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...