Chris Glover Email & Phone Number
Head of R and D Quality Drug Product and Genomic Medicines Unit @ Sanofi
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Chris Glover Location
- Framingham, MA, US
Chris Glover Work
- Head of R and D Quality Drug Product and Genomic Medicines Unit @ (June 2025 - Present)
- Head of R and D Quality Drug Product @ (April 2024 - Present)
- Senior Director Quality @ (May 2021 - April 2024)
- Senior Director Quality Control @ (December 2019 - May 2021)
- Director QA @ (March 2016 - December 2019)
- Director of Quality Control @ (December 2014 - March 2016)
- Associate Director, QA @ (October 2011 - December 2014)
- Head of R and D Quality Drug Product and Genomics Medicines Unit @ sanofi us (May 2025 - June 2025)
- Sr. Manager @ (May 2008 - October 2011)
- Sr. Manufacturing Supervisor @ (May 2007 - May 2008)
- QC Supervisor @ (January 1996 - May 2007)
Chris Glover Education
- BS, Information Technology
BS (Information Technology)
2004-2007 - University of Phoenix
Bachelor's degree (Management Information Systems and Services)
- University of Strathclyde
Master of Science - MS (Pharmaceutical Quality)
Chris Glover Skills
- Data Integrity
- Team Leadership
- Qualified Person
- Cleaning Validation
- Spectroscopy
- Validation
- CAPA
- QC
- Quality Assurance
- Chromatography
- GMP
- Sop
- Quality Control
- FDA
- GLP
- Quality Management
- 21 CFR Part 11
- Quality System
- Quality Auditing
- HPLC
- GxP
- V&V
- Aseptic Processing
- LIMS
- Microbiology
- Standard Operating Procedure (SOP)
- High-Performance Liquid Chromatography (HPLC)
- Corrective and Preventive Action (CAPA)
- U.S. Title 21 CFR Part 11 Regulation
- Laboratory Information Management System (LIMS)
- Verification and Validation (V&V)
- Good Laboratory Practice (GLP)
- U.S. Food and Drug Administration (FDA)
- Lean Manufacturing
- Engineering
- Oversight
- Microsoft Office
- Marketing
- Continuous Improvement
- Inspection
- Verification and Validation V&V
- High Performance Liquid Chromatography Hplc
- u.s. Food and Drug Administration Fda
- Strategy
- Good Laboratory Practice Glp
- Corrective and Preventive Action Capa
- Standard Operating Procedure Sop
- Laboratory Information Management System Lims
- Customer Service
- Standard Operating Procedure
- Corrective and Preventive Action
- High Performance Liquid Chromatography
- Laboratory Information Management System
- Verification and Validation
- u.s. Food and Drug Administration
- Good Laboratory Practice
Chris Glover Summary
- Chris Glover, based in Framingham, MA, US, is currently a Head of R and D Quality Drug Product and Genomic Medicines Unit at Sanofi. Chris Glover brings experience from previous roles at Sanofi. Chris Glover holds a 2004 - 2007 BS in Information Technology @ BS, Information Technology. With a robust skill set that includes Data Integrity, Team Leadership, Qualified Person, Cleaning Validation, Spectroscopy and more. Chris Glover has 3 emails and 3 mobile phone numbers on RocketReach.
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