Quality Jobs
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Sr. Quality Engineer
Position SummaryWe are seeking a Senior Quality Engineer to support quality initiatives across product development, manufacturing, and post-market activities for a growing medical device organization. This individual will partner with cross-functional teams to ensure products consistently meet quality, regulatory, and customer requirements while d...
Quaity Engineer
Join a Growing Medical Device CompanyWe're looking for a hands-on Manufacturing Quality Engineer to play a key role in supporting manufacturing operations, driving quality improvements, and ensuring products meet the highest standards of compliance and performance.This is an excellent opportunity for someone who enjoys solving problems on the manuf...
Senior Design Quality Engineer
Role: Senior Design Quality EngineerSalary: $135k - $155kLocation: Irvine, CA (On-site)EPM is partnered with a growing medical device company in Orange County that's continuing to build out its Quality function and looking to bring in a Senior Design Quality Engineer. This is a high-impact role supporting product development end-to-end, working clo...
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Quality Engineer Metrology
Metrology Quality Engineer (12-Month Contract)📍 France | 🏥 Medical Device ManufacturingWe are supporting a leading medical device manufacturer in their search for an experienced Metrology Quality Engineer to join their site on an initial 12-month contract.This is a high-impact role focused on establishing and developing an on-site Metrology and ...
GMP Qualification & Validation Consultants
Location: Toulouse Area, France Contract: Freelance / Consulting Assignment Industry: Pharmaceutical Manufacturing / CDMO Start: Q3/Q4 2026The ProjectWe are supporting a major pharmaceutical manufacturing site in the Toulouse area that is undergoing significant expansion and operational growth.Multiple projects are running simultaneously across m...
Quality Specialist
Contract DetailsStart Date: ImmediatelyLocation: Montpellier, France (5 days on-site)Hours: 40 hours per week (full-time)Engagement: 6 month Freelance Contract Key ResponsibilitiesEnsure the Quality Management System remains compliant with internal procedures and applicable global regulatory requirements, including ISO 13485, EU MDR, FDA QSR/QMSR, ...
