Part of Phaidon International
Part of Phaidon International
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SAP Integration Lead Start date: ASAP preferredDuration: Long-term programme / renewable contractLocation: Remote-first with flexibility for site engagement.Contract: Contingent / freelance contractTravel: International travel may be required across manufacturing locations.Working pattern: Remote, hybrid, core-hours overlap with Americas teams. A g...
Our client is seeking an experienced External Quality Senior Specialist to support Quality Process & Operations activities within a global pharmaceutical environment. This role focuses on strengthening External Quality processes, supplier oversight, quality systems management, regulatory compliance, and continuous improvement initiatives across ex...
About the OpportunityAn innovative clinical-stage biotechnology company is seeking an experienced Clinical Trial Manager to support the delivery of next-generation therapies and vaccines. This is an opportunity to join a highly collaborative, science-driven environment focused on advancing novel treatment approaches and improving patient outcomes w...
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EPM Scientific is supporting a Global MedTech to hire a Sr. RA Consultant to join their Joint Replacement RA Team, looking for someone with a strong background in EU & US regulations, ideally with Orthopaedics & Sustaining/Change Control experience.This is a 12 month, 4 days per week, remote hourly rate contract, start dates ideally mid-September.J...
Regulatory CMC ConsultantContract: 18 Months Location: Copenhagen, Denmark (Fully Remote) Industry: Vaccines / Global Public HealthWe are supporting a leading pharmaceutical organisation on a high-profile Tuberculosis (TB) vaccine development programme and are looking for an experienced Regulatory CMC Consultant to join the team on an 18-month cont...
EPM Scientific are currently partnered with a clinical-stage biotechnology company focused on innovative therapies for immune-mediated diseases. They are urgently seeking a Director, Medical Writing to support their expanding Clinical Development and Regulatory Affairs team. See a summary of the role below: Role Overview: Start date: ASAPLocation:...