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Role OverviewA freelance QA Manager is required to provide interim support at a GMP‑licensed site specializing in sterile and biologics manufacturing. The consultant will ensure compliance with EU GMP and Annex 1, strengthen quality systems, and prepare the site for upcoming regulatory inspections. Key ResponsibilitiesOversee and maintain site qual...

Overview: This role supports organ transplantation by managing advanced organ preservation and transport technology. The position involves hands-on operation of the system during organ retrieval, preservation, and assessment, ensuring optimal conditions for successful transplantation.Key ResponsibilitiesOperate organ preservation technology during ...

The Senior Process Engineer will lead the design, optimization, and scale‑up of manufacturing processes for advanced drug delivery systems. This role requires proven industry experience in pharmaceutical or biotech manufacturing, with a strong track record of technology transfer, process validation, and GMP compliance. The Senior Process Engineer w...

The Quality Engineer collaborates closely with the engineering team to identify and understand critical-to-quality design attributes and specifications. This role involves reviewing and releasing custom hardware, sub-project, and project DHF documentation to ensure compliance with all applicable regulatory requirements. The individual will contribu...

Regulatory Affairs Consultant - Software as a Medical Device (SaMD) Location: Amsterdam, Netherlands (Remote/Hybrid)Length: 12 monthsStart Date: January 2026 About the RoleWe're looking for an experienced consultant to advise on regulatory and quality strategies for software-driven medical technologies. This role is ideal for someone who understand...