Consultant, Pharmaceutical Services

Phone: +44 (0) 1751 432 999
Country: United Kingdom

Ian Ramsay has 13 years of experience in the pharma biotech industry, most recently as a GMP/GDP inspector with the UK Medicines and Healthcare products Regulatory Agency (MHRA). In this role he was responsible for planning and executing inspections worldwide across a wide range of products and dosage forms. He specialized in data integrity and unlicensed aseptic operations, and also managed serious non-compliance cases through the formal regulatory process (IAG). He is also is experienced in site remediation activities.

Ian also has significant experience within QC and QA. He spent significant time in frontline QA roles supporting a range of products and dosage forms including steriles, non-steriles, tablets, capsules, topicals, injectables, inhaled products and biologics. This role culminated in a global QA function where he spent two years supporting inspection readiness and providing oversite for multiple vaccine manufacturing sites worldwide.

Mr. Ramsay’s areas of expertise include:

  • GMP auditing of facilities and processes
  • Sterile manufacture
  • Microbiology QC
  • Data integrity
  • Unlicensed aseptic manufacture
  • Inspection readiness
  • Remediation