Michael Locke

Senior Director Regulatory, Quality and Medical Emeai

We found the following information about Michael Locke at EUROIMMUN US, where Michael Locke has worked as a Director Of Regulatory Affairs since 2013. Michael's total work experience is over ten years, during which time Michael had at least four jobs at different places to develop professional skills. Michael studied at the Rutgers, The State University of New Jersey-New Brunswick from 2004 to 2008. Currently, Michael lives in New York, New York. You can contact with Michael by looking for phone number or email or find further information by requesting access to this person's further details from us.
Name variants:
Mikael Locke, Mychael Locke, Mike Locke, Mikey Locke, Mick Locke, Mickey Locke, Micky Locke, Michl Locke, Mischa Locke

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Contact Information

Last Update
Jul 5, 2022
Email
lo**@gmail.com
Location
New York, NY
Company

Workplace

EUROIMMUN US
Director Of Regulatory Affairs

Industry

Biotechnology

Work History

Director Of Regulatory Affairs

Morris Plains, NJ
from Mar 2013

Director of Regulatory Affairs

Ocean, New Jersey
•Responsible for the preparation of domestic & international submissions; assuring compliance with foreign regulatory laws. Coordinated submissions through interaction with Research and...
from Apr 2008

Regulatory Affairs/QC & QA Analyst

Manalapan, New Jersey
•Equipment, product & process validation; •Purchasing & QC/Acceptance of all chemicals (raw materials), laboratory supplies, and shipping & receiving supplies; •Sampling and Qua...
Aug 2002 — Apr 2008

Laboratory Tech. (Analyst) Level III

Manalapan, New Jersey
•Oversee all production and formulations in Bacteriology, Immunology, & Serology departments; •Worked with live cultures, blood & blood components; •Aseptic Culture Transfer and Is...
Jun 1998 — Aug 2002

Occupations

Executive
Senior Director
Director
IT Professional
Software Tester
Sales Specialist
Supplier
Accountant
Auditor
Senior Manager
Operations Manager
Computer Specialist
Services Professional
Sales Representative

Skills

Fda
Medical Devices
Gmp
Regulatory Affairs
Validation
Capa
Regulatory Submissions
Quality Assurance
Biotechnology
Iso 13485
Ce Marking
Quality System
Glp
Life Sciences
21 Cfr
Medical Device Directive
V&V
Iso 14971
Fda Gmp
Quality Control
U.s. Food and Drug Administration
Corrective and Preventive Action
Microsoft Excel
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