MSI Pharma are looking to hire two Quality Assurance Specialists (GCP) for one of our long-term Pharma clients based in Belgium. 2 days on-site per week is required for this role.
Main responsibility include:
- Partnering with internal and external business partners to help with driving quality into the clinical development portfolio across the UCB sites and departments and provide Clinical Development Quality input to cross functional teams dealing with complex and/or important projects and issues
- Providing mentoring and guidance to other members of the Clinical Development Quality team, supporting the Global Head and/or Regional Heads by deputizing for them at meetings on request, and contributing to planning and resource prioritization decisions for Clinical Development Quality activities
- Partnering with Development Solutions in driving quality into the clinical activities across the UCB sites
- Providing quality and compliance oversight as well as investigative support to UCB activities regulated by Good Clinical Practices (GCP)
An ideal candidate would have In-depth knowledge and understanding of ICH-GCP, applicable regulations (domestic and international), quality principles, inspection preparation and hosting, risk management and relevant business processes and techniques.
If you are interested please email us or call directly for fast response -
+44 3333 0769 13
As there are 2 openings for this position, please feel free to refer anyone who you think might be a good fit for this role - any recommendation that comes to a deal with be rewarded!
Looking forward to connecting!
