Part of Phaidon International
Part of Phaidon International
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Global Head of Regulatory Affairs A global biopharmaceutical company is seeking 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 programs and...
The OpportunityA growing bio-pharmaceutical company is seeking a Senior Manager, Clinical Quality to provide quality oversight across clinical studies and vendor programs.This role will partner closely with clinical teams, CROs, and vendors to ensure GCP compliance, support inspection readiness, and drive quality throughout the clinical development...
EPM Scientific is partnering with a leading biopharmaceutical organization seeking a Director, Field Effectiveness to join its U.S. Field Excellence team. This highly visible leadership role will guide a team responsible for strengthening field performance across Rare Disease and Oncology while improving the overall experience and effectiveness of ...
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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...
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...
Senior Regulatory Affairs SpecialistWe're hiring a Senior Regulatory Affairs Specialist to support U.S. and global regulatory submissions for medical devices and partner with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.Key ResponsibilitiesPrepare and support submissions including IDEs, 510(k)s, CE Technic...