Biotechnology, AD & QC Strategy, Pre-clinical to Commercialisation, Lab Commissioning & QMS Expert
Hourly rate: members only
Availability: members only
Willingness to travel: Not specified
Professional status: Freelancer
Last updated: 22 Mar 2026
Total work experience:
Language skills: English,
Personal summary
I am a strategic Quality Control and Analytical Development Director with over 18 years of leadership in the biotechnology and pharmaceutical sectors. I have a proven record of managing global cross-functional teams and navigating complex drug development stages from pre-clinical phases through to commercialisation. My expertise includes commissioning GMP laboratories, digitalising systems via Veeva QMS, and leading successful regulatory submissions for the MHRA, FDA, and EMA.
Language skills
English
Native speaker