On Site Manufacturing Jobs
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Manager Program Management
Manager, Program ManagementLocation: Madison, WI Work Model: 100% Onsite Compensation: Competitive base salary + bonus potential + comprehensive benefitsAbout the OpportunityAn expanding biologics CDMO is seeking a Manager of Program Management to lead complex client programs across biologics development and manufacturing. This individual will over...
Senior Automation Engineer
Senior Automation EngineerLocation: Bothell, Washington, USASalary: $185,000 - $200,000 USD + Bonus + Comprehensive BenefitsLead Automation InnovationAre you passionate about robotics, automation, and building the future of advanced medical manufacturing?We are seeking a Senior Automation Engineer to lead high-impact automation initiatives that imp...
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...