Cheryl Brucato

Director, Quality Assurance

Cheryl Brucato is a high-skilled expert, working in Kbi Biopharma main office of which is in 416. on the position of Director, Quality Assurance from 2016. This expert has earned professional experience in more than five positions at different companies. Cheryl Brucato went to the University of Massachusetts Lowell and got education there. Durham, North Carolina is the area, where this professional was lastly known to be settled. This professional's email address and phone number can be easily accessed through SoftwareOfficial on demand.
Name variants:
Cherie Brucato, Cheri Brucato
Last updated Jul 04, 2024

Contact Information

Last Update
Jul 12, 2022
Email
ch**@novartis.com, cb**@aol.com
Location
Durham, NC
Company

Workplace

KBI Biopharma
Director, Quality Assurance

Industry

Biotechnology

Work History

Director, Quality Assurance

1101 Hamlin Rd, Durham, NC 27704
from Sep 2016

Associate Director, Quality Assurance

Formerly Novartis Vaccines (August 2011 - March 2016)
Aug 2011 — Aug 2016

Associate Director, Quality Control

New York, NY
Mar 2006 — Jul 2011

Senior Scientist

225 Binney St, Cambridge, MA 02142
2003 — 2006

Group Leader, Senior Scientist

700 Main St, Cambridge, MA 02139
2001 — 2003

Occupations

Executive
Director
IT Professional
Software Tester
Scientist
Biotechnology Professional
Deputy Director
Operations Manager
Computer Specialist
Biologist
Biological Scientist
Deputy Manager
Chief Executive

Skills

Gmp
Biopharmaceuticals
Gxp
Biotechnology
Lims
Aseptic Processing
Pharmaceutical Industry
Fda
Validation
Quality Assurance
Sop
Glp
V&V
Cleaning Validation
Capa
Regulatory Affairs
Quality System
Clinical Development
Quality Control
Life Sciences
Pharmaceutics
U.s. Food and Drug Administration
Computer System Validation
Gcp
Standard Operating Procedure
Corrective and Preventive Action
Hplc
Lifesciences
Ind
Trackwise
Aseptic Technique
Clinical Trials
Regulatory Requirements
Assay Development
Monoclonal Antibodies
Formulation
Analytical Method Validation
Deviations
Iso 13485
Drug Development
Microbiology
Usp
Good Laboratory Practice
Laboratory Information Management System
Technology Transfer
Verification and Validation
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