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GXPeople are looking for a QMS Engineer to join a well-established Medical Device manufacturer to join their Quality team. About The Role The Quality Management System (QMS) Engineer takes full ...

Knowledge of Medical Device regulations would be advantageous This is a permanent position, hybrid working with Slough based European HQ. This role requires weekley office presence, only considering ...

... Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance * Experience as a Lead Auditor on internal audits and external vendor audits. * Experienced in GxP related CSV audits and ...

Extensive generalist experience in global regulatory affairs within the pharmaceutical, biotech, medical device industry ideally within a dynamic, fast-moving environment. * Extensive knowledge of ...

Have significant sales experience in the medical device industry and cardiology sector * Have a proven track record in developing leads from prospects to closed sales and achieving targets * Have had ...

Responsible for the regulatory compliance of the site according to UK and Ireland regulations for Pharma and Medical Device distribution * Preparation and/or coordination of data and analytics for ...

Their offering is incredibly diverse and would suit someone with experience within either the technology, logistics with an interest in medical or a technical mindset. Genuine career stability and ...