Matthew A German is a high-level professional, that works in Watson Pharmaceuticals as a Cqa Gcp Manager from 2011. This expert has earned professional experience in more than eight positions at different companies. Matthew A German went to the Fairleigh Dickinson University and got education from 2000 to 2002. Outwater, New Jersey is the city, where the professional was lastly known to be settled. Matthew A German's email address and number can be easily accessed through this website on demand.
Name variants:
Mathew German,
Matthieu German,
Matt German,
Mat German,
Matty German,
Mattie German
Last updated Jun 06, 2024
Contact Information
Last Update
Jul 1, 2022
Email
mg**@ptcbio.com, ma**@yahoo.com, ma**@sbcglobal.net
Location
Outwater, NJ
Company
Watson Pharmaceuticals
Workplace
Cqa Gcp Manager
Work History
Associate Director Quality Assurance Gcp Audit
PTC is biopharmaceutical company focused on the discovery and development of orally-administered, proprietary small molecule drugs that target post-transcriptional control processes. While P...
from Mar 2015
Corporate Lead Auditor Gcp
1 Becton Dr, Franklin Lakes, NJ 07417
Develop corporate GCP auditing program for domestic and global clinical operations
Create SOPs and tools for the conduct of GCP study site, internal system and supplier audits
Plan, organ...
Sep 2008 — Sep 2011
Research Quality Auditor
Illinois
· Conduct audits of investigative clinical sites to assess compliance with regulations, guidelines, policies, procedures and sponsor requirements within the US, South America, Asia, and EU....
Sep 2005 — Sep 2008
Quality Auditor
· Plan and execute quality audits as the lead auditor for contract laboratories, manufacturers and material suppliers against GMP, ICH, and ISO guidelines
· Design and conduct internal aud...
May 2004 — Sep 2005
Gmp Auditor
81 Fulton St, Boonton, NJ 07005
· Perform audits of external contract facilities as well as internal laboratory and manufacturing areas
· Review and approval of batch records and laboratory data for active pharmaceutical...
Aug 2003 — May 2004
Quality Auditor
· Perform internal audits of both laboratory and manufacturing facilities in accordance with current GMP
· Validate analytical data for manufacturing batch release
· Review and approval o...
Jan 2003 — Jul 2003
Research Chemist
· Method development and validation of protocols for pharmacopeial studies.
· Investigate out of tolerance results and coordinate with senior scientists for their resolution.
· Generation...
Aug 2000 — Dec 2002
Education
2000 — 2002
1994 — 1997
1988 — 1991
Occupations
Executive
Deputy Director
IT Professional
Software Tester
Manager
Doctor
Neurophysiologist
Oncologist
Deputy Manager
Chief Executive
Computer Specialist
Operations Manager
Neurologist
Medical Practice Professional
Medical Practitioner
Skills
Validation
Sop
Gcp
Pharmaceutical Industry
Fda
Quality Assurance
Quality Auditing
21 Cfr Part 11
Cro
Regulatory Affairs
Clinical Research
Regulatory Submissions
Standard Operating Procedure
Protocol
Regulatory Requirements
Capa
Good Clinical Practice
Glp
Medical Devices
Good Laboratory Practice
U.s. Food and Drug Administration
Corrective and Preventive Action