Permanent Jobs in Irvine
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Head of Global Regulatory Strategy
EPM Scientific are working alongside a global biopharmaceutical company that is seeking a Head of Global Regulatory Strategy to lead regulatory strategy for a high-profile injectable aesthetics portfolio. This individual will provide strategic leadership across both biologic and medical device products, with primary responsibility for neurotoxin pr...
Principal R&D Engineer
Position SummaryThe Principal R&D Engineer provides technical leadership for the development, verification, validation, and commercialization of Class II and Class III medical devices. This individual serves as a subject matter expert responsible for driving complex product development programs from concept through design transfer while ensuring co...
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, ...
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Director Quality
Our client is an innovative Class III medical device company developing and manufacturing life-sustaining technologies that improve patient outcomes worldwide. We are seeking a Director of Quality to lead quality strategy, quality systems, and manufacturing quality across product development and commercial operations.Position SummaryThe Director of...
Principal Quality Engineer
Position SummaryThe Principal Quality Engineer serves as a technical leader within the Quality organization, providing strategic and hands-on support for product development, manufacturing operations, process validation, and quality system compliance. This role partners with cross-functional teams to ensure products are designed, manufactured, and...
Senior Regulatory Affairs Specialist
Senior Regulatory Affairs Specialist Overview Join a growing neurovascular medical device team supporting regulatory compliance and product lifecycle activities for innovative technologies used to treat stroke and other neurovascular conditions. This onsite position (4 days/week) partners closely with engineering, quality, clinical, and commercial ...