- Quality Assurance Manager
QA Manager, Wiltshire, Global Pharmaceutical CompanyQA Manager required for a global Pharmaceutical company to lead the quality assurance staff. This is a permanent role based with an exciting company leading the way in its industry. You will work with the director and provide operational QA service. ...
- Quality Assurance Manager - Oxfordshire
QA Manager, Oxfordshire, Global Pharmaceutical Company QA Manager required for a global Pharmaceutical company to lead the quality assurance staff. This is a permanent role based with an exciting company leading the way in its industry. You will work with the director and provide operational QA service. This is a great opportunity for those in a team leader role to move into management position within QA. ...
- Quality Assurance Manager
Quality Manager, Global Pharmaceutical Company, Oxfordshire Quality Manager is required for a leading Pharmaceutical company to ensure supply chain operations comply with medical device legislation and quality standards. This is an excellent opportunity to progress your career into a management role or build on your current management experience. You will be working directly with the head of quality, leading external supplier audits. ...
- Senior Regional PV Excellence leader
The Senior Regional PV Excellence Leader is responsible for overseeing Pharmacovigilance (PV) activities in EU region. The Senior Regional PV Excellence Leader ensures quality and compliance with PV policies and processes and establishes best practices among Affiliates within their assigned countries/region, while supporting them with the necessary guidance, support, training, and PV information, in order to meet their accountability to comply with global PV Regulations and Roche policies. ...
- Sr Safety Aggreg Report Spec
PURPOSE Apply knowledge and expertise in the area of safety aggregate and benefit risk management documents. Serve as principal owner of Safety Aggregate Reporting and Analytics (SARA) and Benefit Risk Management (BRM) deliverables and mentor less experienced staff. RESPONSIBILITIES Contribute knowledge and expertise to or lead assigned deliverables in the field of SARA and BRM. ...
- Home-based Clinical Project Manager required for Top Global Pharma, UK
Our client is a very successful global pharma, Top pharma company to work for and have cutting edge compounds in the market, they are passionate working in Clinical Research and making a difference on a global scale, they too would like you to have this same passion joining them.
This is a full-time opportunity so if you are a Clinical Research Professional who has a mixed background in both Lead CRA/Project Management experience within UK then please read on…
- Drug Safety Project Manager in Maidenhead, Berkshire
COVANCE - one of the top 5 global Contract Research Organizations in currently looking for its next Project Manager of Drug Safety to join its local team in Maidenhead.
- Senior Regulatory Affairs Specialist - Hampshire - Medical Devices
Our client is an established and growing medical device company based in Hampshire, they are presently recruiting for a Senior RA Specialist / Regulatory Affairs Executive to join their team.
- Senior Regulatory Affairs Specialist \ RA Manager
Senior Regulatory Affairs Specialist \ RA Manager
Hampshire - £50-55kpa. Our Client is an established developer of complex medical devices, they are currently recruiting or a Snr RA Specialist / Regulatory Affairs Manager
- PW 6550 Senior Manager or Associate Director Global QA
This is an opportunity to take responsibility for ensuring high quality consistency of products in both development and commercial stages and contribute to QA support for commercial readiness activity. You will monitor the quality risk for QA of European marketed products in terms of GMP and GDP and well as coordinate Quality Assurance Activities with European manufacturing sites and EU Region Affiliates.