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...
Owlstone MedicalCambridge is well-known for its cluster of Medical Device organisations but this one really is genuinely one of the... Document Management Systems What's in it for you? Employee share options scheme Private medical insurance The Quality...
The One Group, regulatory requirements, and quality standards in the medical device manufacturing industry. Types of Projects likely... to medical device development and manufacturing, such as FDA regulations and ISO 13485. Our Benefits: 26 days' holiday...
Siemensdeliverables, 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...
Gilead, 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...
Gileadif: 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...
Philips