Contract Manufacturing Engineer Jobs
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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 ...
Senior Process Engineer Sterile Polymer (Contract)
OverviewWe are seeking an experienced pharmaceutical engineering professional to lead the development and implementation of a novel aseptic manufacturing process for biodegradable polymer-based implant products.This role will take ownership of process design, equipment integration, supplier coordination, installation activities, and qualification s...
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...
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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...
Business Process Owner
EPM Scientific are supporting a key Pharmaceutical client on their search for a Freelance Business Process Owner who can act as the process owner, taking responsibility for designing, governing and continuously improving master data processes while ensuring master data is properly represented across strategic business initiatives.ResponsibilitiesPr...
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...