Marc Masson Email
Senior GxP Auditor @ Novartis
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Marc Masson Location
- Liège, WAL, BE
Marc Masson Work
- Senior GxP Auditor @ (October 2012 - Present)
- Senior Director, Quality Assurance , GCP and Pharmacovigilance and GLP, Global Quality Assurance @ (May 2010 - September 2012)
- Quality Assurance Auditing Team Leader and Manager @ Eli Lilly (January 2003 - January 2009)
- Team Leader, GMP Quality Assurance @ Lilly Clinical Operations (January 1999 - January 2001)
- Team Leader, GLP Quality Assurance @ Lilly Development Center (January 1996 - January 1999)
- Head, Quality Coordination @ Lilly Development Center (January 1995 - January 1996)
- Head, Clinical Pathology @ Lilly Development Center (January 1993 - January 1995)
- Supervisor - Clinical Pathology @ Continental Pharma - Searle (January 1984 - January 1993)
Marc Masson Education
- Liege University 1981-1983
- University of Liège
licence (Sciences Sanitaires)
1980-1983
Marc Masson Skills
- Result Oriented
- GCP
- Clinical Trials
- PV
- SOP
- GMP
- GLP
- Pharmaceutical Industry
- GxP
- Pharmacovigilance
- CRO
- Clinical Research
- FDA
- Biotechnology
- Regulatory Affairs
- Clinical Development
- Quality Assurance
- Auditing
- Development
- Regulations
- Good Clinical Practice Gcp
- CRO Management
- U.S. Food And Drug Administration Fda
- Audits
- Research
- Toxicology
- Good Clinical Practice
- u.s. Food and Drug Administration
Marc Masson Summary
- Marc Masson, based in Liège, WAL, BE, is currently a Senior GxP Auditor at Novartis. Marc Masson brings experience from previous roles at Grünenthal, Eli Lilly, Lilly Clinical Operations and Lilly Development Center. Marc Masson holds a 1981 - 1983 Liege University. With a robust skill set that includes Result Oriented, GCP, Clinical Trials, PV, SOP and more. Marc Masson has 1 emails on RocketReach.
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