Consultant, NSF Health Sciences Pharma Biotech

Email: pharmamail@nsf.org
Phone: +44(0)1751 432999
Country: France

Jean-Luc Clavelin has over 30 years’ experience in the pharmaceutical industry with Lilly France, a French subsidiary of Eli Lilly & Co.

He has spent considerable time as a technical advisor to start-up facilities in Central and Eastern Europe, the Middle East and North Africa, with responsibility for technology and process transfer and product launch.

Dr. Clavelin’s roles have also included cGMP Compliance Manager at Fegersheim in France, the company’s largest site outside the U.S.  In addition to improving internal quality assurance systems, he led two FDA inspections, which resulted in the approval and launch of two new products in the U.S. More recently, he was Senior Quality Assurance Advisor at Fegersheim, managing a team of 30 and in charge of strategic improvement.

Dr. Clavelin’s areas of expertise include:

  • Quality control and quality assurance, and implementation of quality standards
  • Risk management
  • International inspection requirements
  • Support of manufacturing operations of parenteral pharmaceutical drug products
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