Rose Lopez Email & Phone Number
Sr. Director of Quality and GMP Operations @ Neumedicines Inc.
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Rose Lopez Location
- Denver, CO, US
Rose Lopez Work
- Sr. Director of Quality and GMP Operations @ (April 2014 - Present)
- Sr. Dir. of Quality and GMP Operations @ Neumedicines (January 2014 - January 2015)
- Director of Operations @ (September 2009 - December 2013)
- Senior Consultant @ (February 2008 - July 2009)
- Quality Compliance Manager @ (January 2004 - January 2007)
- Quality Associate III @ Baxter Hemoglobin Therapeutics (January 2000 - January 2003)
- QA @ (January 1997 - January 2000)
- QA compliance associate @ Geneva Pharmaceuticals (January 1995 - January 1997)
- Interim Manager of the Colorado Bioprocessing Center @ (January 1994 - January 1994)
Rose Lopez Education
- Colorado State University
Bachelor of Science (BS) (Biological Sciences)
1986-1989
Rose Lopez Skills
- 21 CFR Part 11
- Aseptic Processing
- Biotechnology
- Biotechnology Industry
- CAPA
- Change Control
- Clinical Development
- Commercialization
- Compliance
- Computer System Validation
- FDA
- GLP
- GMP
- Life Sciences
- Lifesciences
- Operational Excellence
- Operations Management
- Pharmaceutical Industry
- Quality Assurance
- Quality Auditing
- Quality Management
- Quality System
- Regulatory Affairs
- Regulatory Submissions
- SOP
- Technology Transfer
- V&V
- Microsoft Word
- Computer System
- Change Management
- Microsoft Excel
- Operations
- Strategy
- Training
- Research
Rose Lopez Summary
- Rose Lopez, based in Denver, CO, US, is currently a Sr. Director of Quality and GMP Operations at Neumedicines Inc.. Rose Lopez brings experience from previous roles at Neumedicines, Merck, RMC Pharmaceutical Solutions and Amgen. Rose Lopez holds a 1986 - 1989 Bachelor of Science (BS) in Biological Sciences @ Colorado State University. With a robust skill set that includes 21 CFR Part 11, Aseptic Processing, Biotechnology, Biotechnology Industry, CAPA and more. Rose Lopez has 1 emails and 3 mobile phone numbers on RocketReach.
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