Quality Control Manager

Quality Control Manager (QC) - Pharmaceuticals 

Permanent Position 

£40,000 - £45,000 

Based in Kent 

Do you have a scientific background with demonstrable experience in spearheading Quality Control in a Good Manufacturing Practice environment?

Would you like to make an impact contributing to pioneering and exciting Pharmaceutical Chemistry?

My client are an global market-leading manufacturer of unique API's, dedicated to scientific innovation. As a Quality Control Manager, you'll be at the front line of ensuring products meet the highest standards of quality and precision, in the lab leading a team to achieve results. 

Main Duties of the Quality Control Manager (QC) :

• Perform physical and analytical testing following internal methodology to support manufacturing, adhering to stringent GMP criteria to enable the day to day oversight of the QC laboratory.
• Develop SOP's and new techniques to support customers and product excellence. 
• Conduct investigations into Out of Specification results and Non-conformance's. 
• Liaising with QA and management teams to maintain Quality Management Systems are maintained, assuming responsibility for Data management and Stability study.
• Implement regular staff performance reviews for department members to lead and manage staff with assistance from the HR department.
• Coordinate equipment maintenance by external contractors and outsource analysis based on company needs. 

Key requirements and Skills of the Quality Control Manager (QC)  :

• BSc/Msc in a related scientific discipline such as Chemistry, Analytical Chemistry, Pharmaceutical Science or have suitable experience. 
• Proven in-depth record spearheading Quality Control and GMP best practice within a lab environment to ensure compliance and accuracy.
• Excellent problem-solving abilities to permit troubleshooting and support QC staff.
• Conscientious with excellent organisational skills to produce clear and timely QC reports. 
• Strong written and verbal communication abilities to deliver high quality correspondence to cross functional teams would be advantageous.
• Able to regularly commute or relocate to site in Kent, Dover. 

Ready to Lead? We want to hear from you! 

Apply below, or contact Deon at CY Partners for more information. 

Key Words "GMP, Good manufacturing practice, Quality management system, QMS, QC, Quality Control Manager, Pharmaceuticals, API, Active Pharmaceutical Ingredient, Drug Product, excipient Drug Substance, Validation, documentation, problem solving, CAPA, Corrective Action Preventive action, Change control, OOS, Out of Specification, NCW, Non conforming work flow, Kent, Dover, South East"