Flexible Hybrid Compliance Jobs
Showing 21 results
Sort by:
Principal Quality Engineer
Position SummaryThe Principal Quality Engineer is responsible for providing technical leadership and quality engineering expertise across product development, new product introduction (NPI), manufacturing, and post-market activities. This role serves as a key quality representative supporting design control, process validation, risk management, reg...
Principal Engineer, Process Development & Scale-Up
Principal Engineer, Process Development & Scale-UpLocation: Greater Boston Area Base Salary Range: $145,000-$170,000 SummaryWe are currently partnered with a growing life sciences organization developing an innovative combination-product platform.The organization is seeking a Principal Engineer, Process Development & Scale-Up to lead the developmen...
Quality Director
Director of QualityLocation: Minnesota (Hybrid) Industry: Medical DeviceWe are partnering with an innovative medical device company seeking a Director of Quality to lead quality strategy, compliance, and continuous improvement initiatives across the organization.ResponsibilitiesLead and enhance the Quality Management System (QMS) in compliance with...
Elevate your career
Take the first step toward your next opportunity - submit your CV and get started today.

Director of Quality
Role: Director of Quality Location: Irvine, CA (Hybrid) Salary: $180,000 - $225,000EPM is partnered with a rapidly growing medical device company focused on developing breakthrough structural heart technologies to address complex cardiovascular conditions. With strong clinical momentum, expanding commercial adoption, and a robust product pipeline, ...
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 ...
Regulatory Affairs & Quality Consultant
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...
