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Resumes 81 - 90 of 95 |
Fountainville, PA, 18923
... * Made sure the lab is in full GMP compliance by introducing and revising SOPs. * Developed procedures, systems, and practices to ensure compliance to all regulatory requirements. Ajay K. Saini, Ph.D. Page 2 of 3 IVAX Pharmaceuticals, Northvale, NJ ...
- 2011 Apr 19
Hackettstown, NJ, 07840
... • Responsible for the review, routing, distribution and filing of GMP/GLP documentation. Updated and maintained document tracking databases and archival systems. • Prepared, routed, and tracked documentation packages throughout review and approval ...
- 2011 Feb 22
Allentown, PA, 18106
... electronic, electrical and customized repairs, mechanical repairs, including custom fabrication, common metric and standard measurements, mathematical skills required Assign tasks as needed, delegate when appropriate cGMP, GMP, & FDA Documentation; ...
- 2011 Feb 17
Macungie, PA, 18062
... GMP enforcement and documentation . Metal detector and X-Ray setup and HACCP checks . Hazardous Analysis and Critical Control Points (HACCP) paperwork and package verifications, allergen checks . Check water activity and viscosity of products
- 2010 Oct 30
Easton, PA, 18042
... Control Ergonomic Design ISO 9001 GMP's (Good Manufacturing Practices) Master Control FDA Complaint ECN (Engineering Change Notice), Design Control, CAR (Corrective Action Request) FDA Inspection Hazard Communication QSR (Quality System Regulation)
- 2010 Oct 29
Easton, PA, 18045
... Review incoming inspection data a custom parts and resolve quality problems to insure GMP and FDA compliance. Responsible for a number of multi-million dollar projects which included engineering, designing, purchasing parts, fabricating, testing and ...
- 2010 Sep 13
Northampton, PA, 18067
... Work with cross functional teams to ensure that key product issues are identified and communicated to the division for corrective action, especially pertaining to FDA/GMP compliance standards. Issue quarterly executive summary reports on product ...
- 2010 Aug 19
Bethlehem, PA, 18017
Career Synopsis: o Pharmaceutical professional with 13 years experience in all phases of pharmaceutical/biotech research & development o Extensive knowledge of the Code of Federal Regulations including Good Manufacturing Practice (GMP), Good ...
- 2010 Aug 12
Bethlehem, PA, 18020
... Perform metrics on SOPs/LPs processed within the department 2001-2006: Compliance Specialist- GMP . Perform compliance review of SOPs against Level II Standards, . Corporate Polices and GMP/GLPs . Perform SPRISOP and Commander Administrator ...
- 2010 Aug 10
Lehigh Valley, PA, 18002
... perform due diligence on acquisitions, conduct technical training, reduce raw material costs, establish/qualify supply chain, establish/develop new manufacturing sourcing, and assist with GMP compliance for major American and European companies. ...
- 2010 Aug 03