Garrison Beye

Director, Manufacturing and Development

Garrison Beye has been a Director, Manufacturing and Development in Heron Therapeutics, Inc. since 2019. Moreover, Garrison Beye has professional experience at more than six companies in the relevant field. Garrison has a total work experience of 17+ years. Garrison Beye studied at the University of Saskatchewan from 2004 to 2010. Garrison can be found in Berkeley, California – where this professional is currently located. You can find Garrison Beye's actual email address and phone number through Connexy search.
Name variants:
Garrison Beye

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Contact Information

Last Update
Jul 8, 2022
Email
g.**@usask.ca, ga**@bayer.com
Location
Berkeley, CA

Workplace

Heron Therapeutics, Inc.
Director, Manufacturing and Development

Redwood City, CA

Industry

Biotechnology

Work History

Director, Manufacturing and Development

4242 Campus Point Ct SUITE 200, San Diego, CA 92121
from Aug 2019

Associate Director, Quality - Projects and Critical Incidents

Member of the Quality Leadership team for all quality functions for the Bayer Berkeley supply center Managed process that allocated quality personnel to projects Led cross-functional team...
Oct 2018 — Aug 2019

Associate Director, Drug Substance Manufacturing Sciences

Perfusion cell culture and purification process support and optimization for multiple concurrent production processes. Raw materials support and qualification. Leadership of team comprised o...
Jun 2012 — Oct 2018

Director, Research and Development

Product and process development for isolation, purification, and protein hydrolysis of spray-dried protein isolate and hydrolysate (patent: US 9,155,323 B2) Managed: 24/7 on-site pilot pla...
Feb 2010 — May 2012

Manager, Manufacturing Sciences

225 Binney St, Cambridge, MA 02142
Technology transfer from development to manufacturing (PI-IV products) (antibodies: cell culture, purification, and final container) internally and externally (CMOs). Wrote regulatory submis...
2001 — 2004

Manager, Technical Services

Aseptic processing, formulations and lyophilization cycle development of a lyophilized, liposomal parenteral. Technology transfer to CMOs. Process and equipment validation. Wrote CMC section...
1996 — 2001

Education

Occupations

Executive
Director
Deputy Director
Operations Manager
Deputy Manager
Chief Executive

Skills

Technology Transfer
Gmp
Biotechnology
Validation
Biopharmaceuticals
Purification
Fda
Analytical Chemistry
Pharmaceutical Industry
Sop
Change Control
Capa
Chemistry
Drug Development
Science
Chromatography
Aseptic Processing
U.s. Food and Drug Administration
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