- Regulatory Affairs-Medical Devices-10 NEW VACANCIES-Germany
Are you a Regulatory Affairs professional looking for Regulatory Affairs opportunities in Germany? I have a list of OVER 15 POSITIONS here...
- Area Quality Risk Manager for Human Subject Research
Area Quality Risk Manager for Human Subject Research Required for Global Pharma Based in Wavre, Belgium.
- Quality & Risk Manager
A large global pharmaceutical company with leading products across various therapeutic areas are looking to hire a Quality & Risk Manager for contract work based in Belgium or the Netherlands. This is an exciting opportunity to work at an innovative and prestigious top 10 global pharmaceutical company that employs approximately 100,000 people worldwide. ...
- GMA Project Manager
Purpose: The Project Manager (PM) is expected to actively contribute to the development of the medical planning, and then help the teams to effectively and efficiently deliver on the strategic objectives agreed with the relevant governance body (covering both Medical Affairs initiated and non Medical Affairs initiated activities). The PM partners with the International Medical Affairs Team Leader and functional representatives to ensure that project is delivered within timeframes established.
- Sr QA Manager Medical Excellence - The Netherlands (easy commute from Amsterdam) - High Level Re-location Package Available
Sr QA Manager Medical Excellence - The Netherlands - High Level Re-location Package Available...!!!If you wish to apply for this role send your CV with a covering note to email@example.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Matt Greig , in the UK London office, on +44 (0)207 801 3382.
- GMA Project Manager 80%
Purpose: The Project Manager (PM) is expected to actively contribute to the development of the medical planning, and then help the teams to effectively and efficiently deliver on the strategic objectives agreed with the relevant governance body (covering both Medical Affairs initiated and non Medical Affairs initiated activities).
- PW 6129 Senior PV QA Manager / PV Quality Assurance Auditor
Opportunity to join a growing Pharma organisation within a relatively new role strategizing, influencing and implementing global PV programs whilst providing internal and external expert advice. Previous PV Auditing experience is a prerequisite for this role and the position is offered on a permanent, full-time basis.
- Manager Drug Safety, Maidenhead, Berkshire
COVANCE is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.
Right now you can join us as Drug Safety Manager and reinforce our local team in Maidenhead, Berkshire, UK.
- PW 6067 Senior Manager/Associate Director, Quality Assurance Europe
This is an exciting opportunity for an experienced Quality leader (ideally QP) to join an expanding European Quality Assurance group, taking responsibility for GMP and GDP for European marketed and developmental products. Leading and supervising Quality Assurance and Risk Management activities. This is a role offering broad scope at an exciting time in this organisation's growth.
- Medical Director – Pharmacovigilance – UK
Medical Director - Pharmacovigilance - UK
A really exciting role has become available with my client at the Medical Director level. This role will be focused on the Pharmacovigilance services of this CRO and will help the patient safety services grow and develop.