I have an opportunity in the Cheshire region to join a growing bioanalytical research organisation, in a state-of-the-art laboratory providing services to support with discovery and regulatory drug development. If you are a passionate LC/MS specialist wanting to take the next steps into line management then please apply below!
Your Key Responsibilities as Team Leader:
- General management of the team and the projects, to ensure projects are delivered to a high standard to meet deadlines
- Maintain, monitor and review appropriate KPIs
- Working with the business development team to provide expertise to the clients
- Liaise with the QA team to ensure the appropriate regulatory and client audits are scheduled
- Line management of the project leaders, training mentoring and development through appraisals and setting performance targets
- Ensure the team meets financial targets
- Perform technical reviews of plans, results and reports prior to going out to the client. Providing your technical input if necessary
- Authorisation and maintenance of GLP/GCP required documentation
Minimal Requirements:
- 5 + years' experience within a regulatory bioanalytical lab
- PhD or degree within relevant scientific subject, or 10+ years' relevant industry experience
- Experience in a GLP/GCP lab
- Strong bioanalytical project management experience
Additional Skills/ Experience
- Experience using LC-MS/MS, Sciex and Waters LC-MS/MS systems
- Understanding of Analyst, MassLynx, UNIFI, WATSON and SoftMax pro
- Bioanalytical method development and troubleshooting experience
- Method validation experience to FDA/EMA guidelines
- Understanding of Large Molecule analysis and non LC-MS/MS techniques is an advantage
if this opportunity is quite righ for you but you have relevant experienc within the drug discobver industry please send your CV across