On Site Contract Jobs
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Hematology Account Manager Washington/Alaska | CONTRACT
Hematology Account Manager - Washington & Alaska (Contract)Contract Duration: 6-12 Months Compensation: $90-$110/hour + bonus Additional Compensation: Monthly car allowance providedPosition OverviewThe Hematology Account Manager will be responsible for building relationships with hematologists, oncologists, and key accounts to educate them on the p...
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 ...
Scientist Analytical Development
Scientist - Analytical Development (Peptides & New Modalities)Location: Beerse, Belgium (Onsite)Contract: Freelance / ContractOverviewA leading pharmaceutical organisation is seeking a Scientist to join its Analytical Development team in Beerse. This laboratory-based role will support the characterization and development of innovative therapeutics,...
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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...
QA-CSV Specialist & Site Key User
QA-CSV Specialist & Checklyst Manager Site Key UserLocation: Belgium (On-Site) Contract End Date: 31 December 2026 / 2027 ( there is one role ending 2026 and one ending 2027) Function: Quality / Validation Industry: Pharmaceutical ManufacturingAbout the RoleWe are seeking a QA-CSV Specialist & Checklyst Manager Site Key User to support a leading p...
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...