Cpl Life Sciences Vacatures in Nederland

· documentation specialist · Indexing and categorizing of documents · Palletizingofboxes · Coordinate shipmentofdocumentsandretainedsamples ...

Quality Assurance Coordinator · This role is integral in controlling the inspection of incoming materials to support development and manufacturing areas. · Functional testing of devices as it pertains to lot qualification · Packaging integrity testing of devices as procedurally ...

The Associate Documentation will work under the guidance of the Quality Assurance Manager to maintain the Document Control System to ensure control, security, integrity and availability of documentation to site personnel. · ...

I'm working with a Medical Equipment Manufacturing organisation based in Waalwijk, Netherlands in their search for a Quality Assurance Coordinator to join the team. This position will be integral in controlling the inspection of incoming materials to support development and manuf ...

This position will be integral in controlling the inspection of incoming materials to support development and manufacturing areas. · Perform functional testing of devices as it pertains to lot qualification · Maintain and file inspection records and reports. · ...

+This role involves maintaining document control and record retention for a medical device organisation. · +Maintain DHR documentation database. · Control the flow of DHR documents to support lot release, as required. · ...

Quality assurance coordinator to join the team. · ...

Job title: Quality Assurance Coordinator · Job Type: Full-time permanent · Location: Waalwijk, Netherlands – On-site · Cpl Life Sciences is collaborating with a growing Medical Device Organisation who are looking to recruit 4x QA Coordinators. These positions are on-site roles ...

This position will be integral in controlling the inspection of incoming materials to support development and manufacturing areas. · ...

as documentation specialist, you will be responsible for: · palletizing boxes · coordinate shipment of documents and retained samples · perform all duties according to company guidelines with regulatory requirements.qualification/experience required:, ...

A global manufacturer of high-purity chemicals seeks a Business Development Manager to drive growth across Europe within the pharmaceutical, biotech, and medical device markets. · ...

Key Responsibilities: · Maintain DHR documentation database. · Control the flow of DHR documents to support lot release, as required. · Create and update documentation for DHR files & logs. · Filing and other organizational tasks. · Perform Lot Release. · The Associate Documentat ...