Joan Beck Email & Phone Number
Director, Regulatory Affairs @ Phlow
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Joan Beck Location
- Greensboro, NC, US
Joan Beck Work
- Director, Regulatory Affairs @ (January 2022 - Present)
- Regulatory Affairs @ (January 2021 - January 2022)
- Director, CMC Regulatory Affairs @ Kindred Biosciences, Inc. (January 2018 - January 2021)
- Regulatory Affairs CMC @ Elanco US Inc. (March 2015 - January 2018)
- Associate Director Regulatory Affairs @ Novartis Animal Health (September 2012 - March 2015)
- Regulatory Affairs Manager @ Novartis Animal Health (April 2011 - September 2013)
- Regulatory Affairs Product Manager @ (July 2008 - April 2011)
- Quality Assurance Manager @ Boehringer Ingelheim Chemicals, Inc. (November 2006 - January 2008)
- Quality Assurance Supervisor @ Boehringer Ingelheim Chemicals, Inc. (February 2006 - November 2006)
- Quality Assurance Chemist @ Boehringer Ingelheim Chemicals, Inc. (August 2004 - February 2006)
- Quality Control Lab Supervisor @ Boehringer Ingelheim Chemicals, Inc. (November 2001 - August 2004)
- Quality Control Chemist @ Boehringer Ingelheim Chemicals, Inc. (July 1998 - November 2001)
- Engineering Technician @ American Electric Power (January 1988 - August 1994)
Joan Beck Education
- Temple University - School of Pharmacy
Master of Science (M.S.) (Quality Assurance / Regulatory Affairs)
2012-2016 - Virginia Commonwealth University
Bachelor of Science (Chemistry (ACS Certified))
1996-1998 - New River Community College
Associate in Applied Science (Data Processing Technology)
1985-1987
Joan Beck Skills
- Regulatory Affairs
- Pharmaceutical Industry
- FDA
- Quality System
- Change Control
- Pharmaceutics
- Sop
- Quality Control
- Regulatory Requirements
- Quality Auditing
- Regulatory Submissions
- Technology Transfer
- Auditing
- Chemistry
- Analytical Chemistry
- Manufacturing
- Validation
- Quality Management
- HPLC
- Drug Development
- Strategy
- Technical Writing
- Good Manufacturing Practice (GMP)
- Quality Systems
- Corrective and Preventive Action (CAPA)
- Standard Operating Procedure (SOP)
- U.S. Food and Drug Administration (FDA)
- cGMP
- LIMS
- FDA GMP
- GxP
- Trackwise
- IND
- NDA
- SOP development
- Pharmaceuticals
- Compliance
- GMP
- Quality Assurance
- CAPA
- Uvvis
- Standard Operating Procedure Sop
- Strategic Planning
- Corrective and Preventive Action Capa
- Regulatory
- Laboratory
- u.s. Food and Drug Administration Fda
- Corrective and Preventive Action
- Standard Operating Procedure
- u.s. Food and Drug Administration
- Good Manufacturing Practice
Joan Beck Summary
- Joan Beck, based in Greensboro, NC, US, is currently a Director, Regulatory Affairs at Phlow Corp.. Joan Beck brings experience from previous roles at HUVEPHARMA, INC, Kindred Biosciences, Inc., Elanco US Inc. and Novartis Animal Health. Joan Beck holds a 2012 - 2016 Master of Science (M.S.) in Quality Assurance / Regulatory Affairs @ Temple University - School of Pharmacy. With a robust skill set that includes Regulatory Affairs, Pharmaceutical Industry, FDA, Quality System, Change Control and more. Joan Beck has 2 emails and 2 mobile phone numbers on RocketReach.
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