Part of Phaidon International
Part of Phaidon International
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Process Validation Engineer IIFargo, ND (Relocation Available) | OnsiteI'm partnering with a rapidly growing biotech/CDMO organization supporting the development and commercialization of cutting-edge therapies and currently seeking a Process Validation Engineer II to join their Technical Operations team.This individual will play a key role in proce...
EPM Scientific are working alongside a growing pharmaceutical manufacturing organization who are seeking a Director of Quality Control to lead QC operations across a GMP-regulated manufacturing site. This individual will provide leadership for laboratory operations and quality control strategy, overseeing analytical chemistry, microbiology, enviro...
Senior Director, Quality Lenoir, NC | Pharmaceutical Manufacturing | OnsiteA global biopharmaceutical manufacturer is seeking a Senior Director, Quality to lead Quality Operations across the U.S. organization. This individual will provide leadership across Quality Assurance, Quality Control, Quality Compliance, Product Release, Supplier Quality, an...
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Manufacturing EngineerMedemblik€75,000 - €80,000 + Bonus + Excellent Benefits PackageAre you a Manufacturing Engineer with experience in production environments?Do you want a role that offers international exposure and the freedom to implement new ideas, where you will see the impact of your work across multiple sites worldwide?On offer is an oppor...
Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...
OverviewWe are seeking experienced quality professionals to support a major pharmaceutical manufacturing client in Greenville, North Carolina. This engagement focuses on strengthening quality oversight, manufacturing compliance, remediation activities, and inspection readiness efforts within a regulated GMP environment.Consultants will join an esta...