MEDICAL DEVICE COMPLIANCE SYSTEMS jobs in CAMBRIDGESHIRE, United Kingdom

as possible. We are looking for a full-time creative and hands-on medical device compliance, systems and engineering change support administrator... is deeply passionate about systems and compliance within the medical equipment sector. Key responsibilities, duties and tasks...

Device QA department Working knowledge, within Pharmaceutical/Medical Device business) of GxP and Quality related...Owlstone Medical’s mission is to change the way we currently diagnose and monitor serious disease; our vision...

lead auditor (internal audits) Experience/ Knowledge Suitable working knowledge within a Pharmaceutical/Medical Device... QA department Working knowledge, within Pharmaceutical/Medical Device business) of GxP and Quality related regulations...

innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank... pathology of interest. Requirements Contribute to the development, maintenance, and compliance of the Quality Management...

, medical device expertise and PS systems. This role is part of the Standards & Inspection Readiness Team, which is the team... experience working with drug safety / PV or related systems, databases, and tools. Strong analytical thinking skills...

deliverables, medical device expertise and PS systems. This role is part of the Standards & Inspection Readiness Team...) checks for ICSRs to ensure accuracy and compliance with Gilead conventions and regulatory standards. Develops and/or assists...

to: * Understand the technology, products and application solutions that FLusso develops. Specify, design and build systems.... Responsibilities New product (and device) development and introduction Building a full understanding of Flusso sensor devices...

if: You’ve acquired 2+ years of experience in medical device or another regulated industry and in the application of automated technology...; understanding of and application of global medical device regulations/requirements and standards including: FDA’s 21 CFR 820, ISO...

to support with FDA approvals. You will receive support from the Quality Systems Manager and play an integral role as a valued...), Device Master Records (DMR), Risk Management Files (RMF), and Device Master Files (DMF) in accordance with procedures...