Experience

Ennogen

• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Head of Quality for Ennogen

  • Jun 2022 - Present



Church & Dwight Co., Inc.

• United States
• Manufacturing
• 700 & Above Employee

• EMEA Business Quality Head

  • Apr 2021 - Jun 2022

• European Head of Quality

  • May 2020 - Apr 2021



Aesica Pharmaceuticals Ltd

• United Kingdom
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Quality Control Manager

  • Jun 2018 - May 2020



CooperVision

• United States
• Medical Equipment Manufacturing
• 700 & Above Employee

• Senior Quality Manager

  • Jan 1998 - May 2017

  CooperVision acquired Sauflon in August 2014, employment started with Sauflon in January 1998 and continued through acquisition. I left CooperVision in May 2017 to take a break and rebalance life, plus also to lay a patio and landscape the garden (which is looking great now). Worked as the Quality Manager for just over 10 years within a very challenging environment with respect to QMS adoption and utilisation. CooperVision acquired Sauflon in August 2014, employment started with Sauflon in January 1998 and continued through acquisition. I left CooperVision in May 2017 to take a break and rebalance life, plus also to lay a patio and landscape the garden (which is looking great now). Worked as the Quality Manager for just over 10 years within a very challenging environment with respect to QMS adoption and utilisation.



Sauflon Pharmaceuticals

• Ashford, Kent

• Chemistry Laboratory Manager

  • Jul 2001 - Feb 2007

  Overall responsibility for the management and smooth running of the Quality Control Chemistry Laboratory and the team of five analysts in the analysis of incoming chemical raw materials and finished product. Ensuring testing was conducted and any issues resolved within key product release target timelines. Development and implementation of a suite of core processes and procedures to improve the reliability and control of the lab equipment in compliance with GMP, GCLP, and Health and Safety (COSHH) requirements to remain audit ready. Fully reviewed and validated/verified all methods, instruments, and equipment from the ground up and implemented a rolling programme to maintain their validated and controlled status.