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Expired
  • Location: Loughborough
  • Salary: Highly competitive salary + benefits
  • Job Type:Permanent

Posted over 1 year ago

Are you an analytical chemistry professional looking to join a highly respected and innovative globally recognised pharmaceutical manufacturing company?
 
Do you want to be a key member of a team that is dedicated to producing top-quality products and driving continuous improvement?
 
If so, we have the perfect opportunity for you!
 
As the Analytical Team Leader, you will have the opportunity to make a significant impact on the analytical team and contribute to the success of our organization. The main responsibilities are as follows:
 
  • Providing technical and operational leadership, management, training, and coaching to Technical Leaders, Senior Analysts, Analysts, and Technicians
  • Taking ownership of the analytical activities required as part of your assigned projects, including identifying technical problems and developing solutions
  • Supporting business development efforts and participating in internal and external visits
  • Communicating any changes to project scope to the Project Manager in a timely manner
  • Implementing and monitoring systems and processes in the Laboratory to ensure compliance with cGMP standards
  • Reviewing and approving protocols, reports, and other project-related documentation
  • Leading the investigation of SAR issues and ensuring they are handled in accordance with procedures
  • Ensuring that the team adheres to Quality Management System document closure timelines
 
As a member of the team, you will have the chance to work with cutting-edge technology and contribute to the development of life-saving products. You will be part of a collaborative and driven team that values continuous learning and professional growth.
 
The main requirements you need to apply are as follows:
 
  • BSc, MSc, or PhD in chemistry, or Life Science subject with a significant chemistry component
  • Significant experience of :
    • Stability study design and testing
    • HPLC method Development
    • HPLC method Validation
    • Dissolution Method Development
    • Dissolution Method Validation
    • Modern Chromatography Software
  • Track record of line managing 10+ staff in a cGMP environment
  • Significant experience of analysing and leading analytical development activities for Pharmaceutical drug products in a GMP environment
 
If you are ready to take on this exciting and challenging role, we encourage you to apply.
 
Please note that this position may require availability outside of normal working hours. It is a requirement of your employment that you are able to fulfill this aspect of the role. All candidates must have the RTW in the UK.