Lee A. Remon Email & Phone Number
Associate Director GMP Quality Assurance @ BBOT
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Lee A. Remon Location
- Wesley Chapel, FL, US
Lee A. Remon Work
- Associate Director GMP Quality Assurance @ (September 2025 - Present)
- Associate Director QA Operations @ (August 2021 - December 2024)
- Sr Regulatory Project Manager @ (February 2019 - September 2021)
- Global Corporate Quality Manager @ (July 2014 - February 2019)
- Director, Quality @ (July 2011 - July 2012)
- Sr. QA Technical Specialist and Project Manager @ Catalent Phama Solutions (July 2007 - June 2010)
- Corporate Technical Project Manager- Global @ Catalent Phama Solutions (May 2005 - January 2008)
- Sr. QA Technical Review Specialist @ Catalent Phama Solutions (December 2001 - April 2005)
Lee A. Remon Education
- University of South Florida
BS (Life Science (Microbiology with emphasis on molecular genetics))
1990-1995
Lee A. Remon Skills
- 21 CFR Part 11
- Analytical Chemistry
- Aseptic Processing
- Aseptic Technique
- Auditing
- Biopharmaceuticals
- Biotechnology
- Business Cycle
- Business Planning
- Business Process Automation
- Business Process Design
- Business Process Improvement
- CAPA
- CRO
- Change Control
- Chemistry
- Cleaning Validation
- Clinical Development
- Clinical Operations
- Clinical Research
- Clinical Trials
- Communication
- Compliance Regulations
- Computer System Validation
- Construction Management
- Continuous Improvement
- Corrective and Preventive Action (CAPA)
- Cross-functional Team Leadership
- Data Management
- Documentation
- Drug Development
- Drug Discovery
- Engineering Management
- FDA
- FDA GMP
- Formulation
- GAMP
- GLP
- GMP
- Global Regulatory Compliance
- GxP
- ICH
- ISO 13485
- ISO 9001
- Inspection
- Internal Audits
- Investigation
- Key Performance Indicators
- LIMS
- Leadership
- Lean Process Improvement
- Life Sciences
- Management Software
- Manufacturing
- Manufacturing Operations
- Manufacturing Operations Management
- Medical Devices
- Mitigation Strategies
- Pharmaceutical Industry
- Pharmaceutical Manufacturing
- Pharmaceutical Research
- Process Improvement
- Product Development
- Product Management
- Product Strategy
- Program Management
- Project Management
- Quality Assurance
- Quality Auditing
- Quality Control
- Quality Management
- Quality Risk Management
- Quality System
- Regulatory Affairs
- Regulatory Compliance
- Regulatory Reporting
- Regulatory Requirements
- Regulatory Submissions
- Resource Allocation
- Risk Management
- SOP
- Skilled Multi-tasker
- Software Documentation
- Software Project Management
- Software Quality Assurance
- Software Testing
- Stakeholder Engagement
- Sterilization
- Strategy
- Supplier Evaluation
- Technical Writing
- Technology Transfer
- Testing
- Trackwise
- U.S. Food and Drug Administration (FDA)
- V&V
- Vaccines
- Validation
- Vendor Management
Lee A. Remon Summary
- Lee A. Remon, based in Wesley Chapel, FL, US, is currently a Associate Director GMP Quality Assurance at BBOT. Lee A. Remon brings experience from previous roles at Sage Therapeutics, Paragon BioTeck, Inc., Syneos Health Clinical Solutions (Previously INC Research/inVentiv Health) and CoreRx, Inc.. Lee A. Remon holds a 1990 - 1995 BS in Life Science (Microbiology with emphasis on molecular genetics) @ University of South Florida. With a robust skill set that includes 21 CFR Part 11, Analytical Chemistry, Aseptic Processing, Aseptic Technique, Auditing and more. Lee A. Remon has 2 emails and 2 mobile phone numbers on RocketReach.
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