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Principal Quality Engineer
Minneapolis$140,000 - $170,000 USD a year

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
Boston$145,000 - $170,000 USD a year

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
$180,000 - $220,000 USD a year

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...

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Selby Jennings Start Your Career In Recruitment
Director of Quality
Irvine$180,000 - $225,000 USD a year

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
Galway

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
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...