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Sustaining Engineer Technician
Sustaining Engineering Technician Innovative Medical Device Company | Hands-On Engineering RoleJoin a growing medical device company developing life-changing technologies. This is a highly hands-on opportunity supporting product testing, prototype builds, failure investigations, manufacturing readiness, and continuous product improvement. What You'...
Director Regulatory Affairs
Director, Regulatory AffairsUSA (Remote)$190,000 - $240,000 Job DescriptionEPM is partnered with an exciting, venture-backed neuromodulation company developing next-generation implantable technologies to treat neurological disorders and improve patient outcomes. With strong financial backing, a growing clinical pipeline, and several key milestones ...
Principal R&D Engineer
An exciting opportunity to lead a growing R&D function focused on the development and commercialisation of innovative interventional medical devices. This role will oversee product development activities from concept through to manufacturing transfer while leading a multidisciplinary team of Engineers, Technicians and Team Leaders.Key Responsibilit...
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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...
Principal Reg Specialist
Influence Regulatory Strategy for Products That Reach Global MarketsThe OpportunityA global medical device manufacturer is looking for a Regulatory Affairs Specialist to join a well-established regulatory team supporting a diverse product portfolio.This is a role for someone who wants to move beyond transactional regulatory work and become a valued...
Senior Regulatory Affairs Specialist
A growing medical device company is seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy and submissions across a diverse product portfolio. This role will partner cross-functionally with quality, clinical, and product development teams to ensure compliance with applicable regulations throughout the product lifecycle...