Professional Records
Lawyers & Attorneys
Dennis Hatkin Phones & Addresses
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Florence, SC
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293 Main St, Chester, NJ 07930 (908) 879-2162 (908) 879-5757
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289 Main St, Chester, NJ 07930
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293 Main St, Chester, NJ 07930 (908) 528-3332
Work
Company:
Bausch health companies inc. Sep 2018
Position:
Labeling manager regulatory affairs
Education
School / High School:
Bloomfield High School
Skills
Fda • Pharmaceutical Industry • Gmp • Sop • Regulatory Affairs • Validation • Capa • Packaging • Cross Functional Team Leadership • Pharmaceutics • Change Control • Quality Control • Trackwise • R&D • Manufacturing • Regulatory Submissions • Six Sigma • Product Launch • Medical Devices • Product Development • Quality System • Software Documentation • Quality Assurance • 21 Cfr Part 11 • Regulatory Requirements • U.s. Food and Drug Administration • Standard Operating Procedure • Iso 13485 • Gxp • Aseptic Processing • Biotechnology
Industries
Pharmaceuticals
Resumes
Resumes
Labeling Manager Regulatory Affairs
View pageLocation:
293 Main St, Chester, NJ 07930
Industry:
Pharmaceuticals
Work:
Bausch Health Companies Inc.
Labeling Manager Regulatory Affairs
Tris Pharma Aug 2017 - Aug 2018
Labeling Manager Regulatory Affairs
Mylan Apr 2013 - Apr 2017
Labeling Manager Regulatory Affairs
Valeant Pharmaceuticals Aug 2012 - Mar 2013
Senior Labeling Specialist
Merck 1999 - 2010
Senior Packaging Engineer
Labeling Manager Regulatory Affairs
Tris Pharma Aug 2017 - Aug 2018
Labeling Manager Regulatory Affairs
Mylan Apr 2013 - Apr 2017
Labeling Manager Regulatory Affairs
Valeant Pharmaceuticals Aug 2012 - Mar 2013
Senior Labeling Specialist
Merck 1999 - 2010
Senior Packaging Engineer
Education:
Bloomfield High School
Montclair State University
Bachelors, Bachelor of Arts, Fine Arts
Montclair State University
Bachelors, Bachelor of Arts, Fine Arts
Skills:
Fda
Pharmaceutical Industry
Gmp
Sop
Regulatory Affairs
Validation
Capa
Packaging
Cross Functional Team Leadership
Pharmaceutics
Change Control
Quality Control
Trackwise
R&D
Manufacturing
Regulatory Submissions
Six Sigma
Product Launch
Medical Devices
Product Development
Quality System
Software Documentation
Quality Assurance
21 Cfr Part 11
Regulatory Requirements
U.s. Food and Drug Administration
Standard Operating Procedure
Iso 13485
Gxp
Aseptic Processing
Biotechnology
Pharmaceutical Industry
Gmp
Sop
Regulatory Affairs
Validation
Capa
Packaging
Cross Functional Team Leadership
Pharmaceutics
Change Control
Quality Control
Trackwise
R&D
Manufacturing
Regulatory Submissions
Six Sigma
Product Launch
Medical Devices
Product Development
Quality System
Software Documentation
Quality Assurance
21 Cfr Part 11
Regulatory Requirements
U.s. Food and Drug Administration
Standard Operating Procedure
Iso 13485
Gxp
Aseptic Processing
Biotechnology