Contract Manufacturing Jobs
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External Quality Senior Specialist
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...
Senior CQV Engineer
Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...
DP MSAT Consultant
Senior Drug Product MSAT / Tech Transfer Consultant (Contract) Location: RemoteStart Date: November 2026Duration: 12 Months (to November 2027)Commitment: Approximately 25 hours per week Overview We are seeking an experienced Drug Product MSAT / Technology Transfer Consultant to support a high-profile CMC programme involving the transfer, scale-up a...
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C&Q Engineer
We are seeking an experienced Commissioning & Qualification (C&Q) Engineer to support ongoing qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. The successful candidate will play a key role in coordinating qualification documentation, executing qualification activities, and ensuring alignment b...
QMS Consultant
OverviewWe are seeking an experienced Quality Systems Manager to lead and continuously improve the Quality Management System (QMS) within a GMP-regulated pharmaceutical environment. This role will be responsible for ensuring compliance with global regulatory requirements while driving quality excellence across manufacturing, laboratory, supply chai...
Asset CQV Engineer
Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...
