Part of Phaidon International
Part of Phaidon International
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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...
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...
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...
Develop and execute Medical Information strategies , including annual planning, launch support activities, insights analysis, response development, review, and approval management.Lead strategic publication planning across assigned products, creating and maintaining annual publication plans based on stakeholder input, study data, scientific eviden...
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...