Will Nelson Email & Phone Number
Sr. Director Quality and Regulatory Affairs @ AZIsotopes
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Will Nelson Location
- Stilwell, KS, US
Will Nelson Work
- Sr. Director Quality and Regulatory Affairs @ (December 2024 - Present)
- Owner @ (January 2024 - Present)
- Principal Scientist, CMC @ (January 2015 - December 2023)
- Pharmaceutical QA Consultant @ (March 2011 - December 2014)
- Manager, API Quality Control @ (April 2010 - February 2011)
- Director of Quality and Regulatory Affairs @ Cedarburg Hauser Pharmaceuticals, Inc. (March 2009 - February 2010)
- Manager, Pharmaceutical QA @ (October 2005 - March 2009)
- QA Manager @ (August 2002 - September 2005)
- QA Manager @ Restoragen (BioNebraska) (May 2001 - July 2002)
- Senior Scientist @ Oread (December 1996 - April 2001)
- Senior Scientist @ Hauser (August 1995 - December 1996)
- Scientist @ Oread (September 1991 - August 1995)
- Chemist @ ChemSyn Science Labs (February 1989 - September 1991)
- Laboratory Manager @ Pennfield Chemical Corp. (July 1987 - October 1988)
Will Nelson Education
- University of Nebraska-Lincoln
Bachelor of Science (Chemistry)
1981-1986
Will Nelson Skills
- 21 CFR Part 11
- Analytical Chemistry
- Biotechnology
- CAPA
- CMC Regulatory Affairs
- Change Control
- Chemistry, Manufacturing, and Controls (CMC)
- Cleaning Validation
- Collaborative Work
- Compliance Remediation
- Consent Decree
- Corrective and Preventive Action (CAPA)
- Documentation
- Drug Development
- Drug Discovery
- Electronic Common Technical Document (eCTD)
- Equipment Qualification
- External Audits
- FDA
- GLP
- GMP
- Global Health
- Good Laboratory Practice (GLP)
- GxP
- ICH
- Investigational New Drug Application (IND)
- Manufacturing Processes
- Pharmaceutical Industry
- Pharmaceuticals
- Pharmaceutics
- Process Validation
- Quality Assurance
- Quality Auditing
- Quality Control
- Quality Management
- Regulatory Affairs
- Regulatory Compliance
- Regulatory Requirements
- Regulatory Submissions
- Research Skills
- SOP
- Small Molecules
- Standard Operating Procedure (SOP)
- Supplier Quality
- Technology Transfer
- U.S. Food and Drug Administration (FDA)
- U.S. Title 21 CFR Part 11 Regulation
- V&V
- Validation
- Standard Operating Procedure
- u.s. Food and Drug Administration
- Corrective and Preventive Action
- Good Laboratory Practice
Will Nelson Summary
- Will Nelson, based in Stilwell, KS, US, is currently a Sr. Director Quality and Regulatory Affairs at AZIsotopes. Will Nelson brings experience from previous roles at PrairiePharmQuality, LLC, Cardinal Health Regulatory Sciences, Validant and Aptuit. Will Nelson holds a 1981 - 1986 Bachelor of Science in Chemistry @ University of Nebraska-Lincoln. With a robust skill set that includes 21 CFR Part 11, Analytical Chemistry, Biotechnology, CAPA, CMC Regulatory Affairs and more. Will Nelson has 3 emails and 4 mobile phone numbers on RocketReach.
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