2009 -
2013 Braine Site Process Validation Associate Director @
2008 -
2009 QA Associated Director, Lab Compliance and Quality Systems @
2007 -
2008 QC Biochemistry Manager @
2002 -
2007 QA Supervisor for QC Labs @
1999 -
2000 QC Analyst @
Frederic Constant Education
University of Liège
Master (Chemical)
1993
-
1998
Frederic Constant Skills
Process Validation
QC
Quality Systems
Quality Assurance
Computer System Validation
GxP
GMP
21 CFR Part 11
cGMP
Validation
CAPA
SOP
FDA
Pharmaceuticals
Change Control
Quality Management
Documentum
Life Sciences
Continuous Improvement
Six Sigma
Lean Manufacturing
Compliance
Process Improvement
Documentation
People Management
Cleaning Validation
GAMP
Change Management
HPLC
Coaching
Quality Auditing
Risk Management
Vaccines
Biopharmaceuticals
Analytical Chemistry
Aseptic Processing
Pharmaceutical Industry
V&V
Quality Control
Quality System
Equipment Qualification
Regulatory Affairs
Technology Transfer
Analytical Method Validation
Regulatory Requirements
USP
Corrective and Preventive Action Capa
Business Analysis
u.s. Food and Drug Administration Fda
Operations
Strategic Planning
Corrective and Preventive Action
u.s. Food and Drug Administration
Frederic Constant Summary
Frederic Constant, based in Liège, WAL, BE, is currently a Liège Site Quality Director at BVI Medical. Frederic Constant brings experience from previous roles at Mithra and UCB. Frederic Constant holds a 1993 - 1998 Master in Chemical @ University of Liège. With a robust skill set that includes Process Validation, QC, Quality Systems, Quality Assurance, Computer System Validation and more. Frederic Constant has 2 emails on RocketReach.
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