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Database & Data Migration Consultant
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...
Senior Mechanical Engineer Fluidics & Disposables
Senior Mechanical Engineer - Fluidics & Disposable Medical DevicesContract DetailsLocation: Limerick, Ireland (On-site)Contract Type: Freelance / ContractorDuration: Initial 12-Month ContractStart Date: ASAPOverviewWe are supporting a leading medical device manufacturer in Limerick that is seeking an experienced Senior Mechanical Engineer to join a...
Regional Director, Field Medical Affairs
Regional Director, Field Medical AffairsLocation: Remote, United States (East Region)About the OpportunityA rapidly growing biopharmaceutical organization is seeking a Regional Director, Field Medical Affairs to lead its East Region field medical team. This is a high-impact leadership role responsible for driving scientific engagement, overseeing a...
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Sustaining Engineer
Sustaining Engineer | Medical Device IndustryJoin a growing medical device company where you'll play a key role in supporting and improving products that make a real impact on patient care. This is a highly visible position offering exposure to product development, manufacturing, quality, regulatory, and supplier management activities. What You'll ...
Product Dev Engineer
Product Development Engineer - Cutting-Edge MedTechJoin a rapidly advancing medtech team delivering breakthrough, minimally invasive technologies that are redefining standards of care in cardiovascular treatment. What you'll do:Own V&V testing, prototyping, and hands-on lab workDrive development from concept through product launchContribute to desi...
Quality Director
Position SummaryThe Quality Director provides strategic and operational leadership for the Quality organization within a regulated medical device manufacturing environment. This role is responsible for ensuring the effectiveness of the Quality Management System (QMS), maintaining global regulatory compliance, driving continuous improvement initiati...