Diana McClellan Email & Phone Number
Associate Director, GMP QA @ PMV Pharmaceuticals, Inc.
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Diana McClellan Location
- Philadelphia, PA, US
Diana McClellan Work
- Associate Director, GMP QA @ (April 2025 - Present)
- Associate Director Quality Assurance @ (January 2024 - April 2025)
- Associate Director Quality Assurance @ (June 2022 - January 2024)
- Associate Director Quality Assurance @ (December 2020 - June 2022)
- Associate Director, 3rd Party Quality Operations @ (August 2018 - October 2020)
- Manager, 3rd Party Quality Operations @ (April 2016 - August 2018)
- Quality Assurance Manager @ (August 2011 - April 2016)
- Quality Project Manager @ (July 2010 - August 2011)
- Quality Assurance Engineer @ (May 2008 - July 2010)
- QA Auditor (ASQ CQA) @ (October 2006 - March 2008)
- QA Specialist III @ MedImmune Vaccines (October 2001 - September 2006)
- Lead QA Compliance Auditor @ Delavau (September 2000 - October 2001)
- QA Associate @ Biovail (October 1998 - September 2000)
Diana McClellan Education
- Virginia Tech
Bachelor's degree (Biochemistry)
1993-1998 - Virginia Tech
Bachelor of Science - BS (Biochemistry)
1993-1997
Diana McClellan Skills
- Aseptic Processing
- Aseptic Technique
- Auditing
- Biopharmaceuticals
- CE marking
- CQA
- Calibration
- Change Control
- Cleaning Validation
- Clinical Trials
- Complaint Management
- Design Control
- Design of Experiments
- FDA
- FDA GMP
- FMEA
- GAMP
- GLP
- GMP
- GxP
- ISO
- ISO 13485
- Medical Devices
- Pharmaceutical Industry
- Process Simulation
- Process Validation
- Product Launch
- Product Quality
- Project Management
- Quality Assurance
- Quality Auditing
- Quality Control
- Quality Management
- Quality System
- R&D
- Regulations
- Regulatory Affairs
- Regulatory Requirements
- Regulatory Submissions
- Risk Management
- Root Cause Analysis
- Sop
- Supplier Quality
- Technical Transfer
- Technology Transfer
- Third Party Vendor Management
- Trackwise
- V&V
- Validation
- Vendor Management
- CAPA
- 21 CFR Part 11
- ISO 14971
- Computer System Validation
- Biotechnology
- Lifesciences
- Biomedical Engineering
- 21 CFR
- LIMS
- Minitab
- Iso 9000
- Operations
- Computer System
Diana McClellan Summary
- Diana McClellan, based in Philadelphia, PA, US, is currently a Associate Director, GMP QA at PMV Pharmaceuticals, Inc.. Diana McClellan brings experience from previous roles at Bristol Myers Squibb, Mirati Therapeutics, Rocket Pharmaceuticals and Sandoz. Diana McClellan holds a 1993 - 1998 Bachelor's degree in Biochemistry @ Virginia Tech. With a robust skill set that includes Aseptic Processing, Aseptic Technique, Auditing, Biopharmaceuticals, CE marking and more. Diana McClellan has 3 emails and 1 mobile phone numbers on RocketReach.
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