Tom Mcgrady

Vice President Quality Assurance

Tom Mcgrady is a qualified professional, working in Tersera Therapeutics main office of which is in 34. on the position of Vice President Quality Assurance since 2017. This expert gained professional experience in more than six positions at various companies. Tom Mcgrady went to the University of Illinois at Chicago and was studying. Northbrook, Illinois is the city, where the professional was known to be living. This expert's email address and phone number are accessed through this website by request.
Name variants:
Thomas Mcgrady

Contact Information

Last Update
Jul 6, 2022
Email
tm**@tersera.com, to**@comcast.net, tm**@pharma-start.com
Location
Northbrook, IL
Company
Tersera Therapeutics

Workplace

Vice President Quality Assurance

Work History

Vice President Quality Assurance

520 Lake Cook Rd SUITE 500, Deerfield, IL 60015
TerSera Therapeutics is a new specialty therapeutics company established in February 2016 with both marketed and pre-market products for the US, Canada, and EU. As the company quality manage...
from Jun 2017

Vice President, Quality and Regulatory Compliance

2100 Sanders Rd SUITE 190, Northbrook, IL 60062
VP, Quality and Regulatory Compliance at Pharma Start, LLC
Apr 2013 — Jun 2017

Director, Quality Assurance and Regulatory Affairs

May 1, 2012 — Mar 1, 2013

Director, Global It Quality

1 Baxter Pkwy, Deerfield, IL 60015
2010 — 2012

Associate Director, Qa

1 Astellas Way, Northbrook, IL
2006 — 2010

Vice President

175 east Hawthorn Pkwy SUITE 210, Vernon Hills, IL 60061
2000 — 2006

Occupations

Executive
Vice President
IT Professional
Software Tester
Representative
Sales Specialist
Supplier
Chief Executive
Computer Specialist
Services Professional
Sales Representative

Skills

Fda
Validation
Gmp
Capa
Pharmaceutical Industry
Change Control
Quality Assurance
21 Cfr Part 11
Quality System
Regulatory Affairs
Sop
V&V
Computer System Validation
Quality Auditing
Biotechnology
Medical Devices
Regulatory Requirements
Cleaning Validation
Gxp
Iso 13485
Gcp
Quality Control
Process Improvement
Regulatory Submissions
Glp
Technology Transfer
Aseptic Processing
Biopharmaceuticals
Clinical Trials
Pharmaceutics
R&D
Lifesciences
Clinical Development
Software Documentation
Inspection
Compliance
Life Sciences
Quality Management
Manufacturing
Design Control
Cro
Hplc
Ind
Iso 14971
Quality Systems
Analytical Chemistry
Cgmp
Pharmaceuticals
Iso 9000
Process Validation
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