Description
evaluates Reviews and approves change control validation protocols and reports to all manufacturing processes as blending granulation compressing coating and printing. Maintains documents in an organized and traceable manner. * Provides advice and service to all operating departments as to assure compliance with cGMP's and other regulations. This includes frequent feed back on performance regarding deviations rejections complaints outstanding commitments trend etc.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Mentor Technical Group | Sr. Quality Assurance Specialist | 2/2018 - 8/2018 |
| Quality Consulting Group | Non Conformance Evaluator | 6/2017 - 9/2017 |
| Conde Indu Services | Sr. Qa Specialist | 6/2015 - 5/2017 |
| Mc Neil Consumer Healthcare (J&J) | Sr. Quality Complaints Coordinator | 1/2012 - 1/2015 |
| Technical Services Results Driven (Tsrd) Corp. | Sr. Technical Services Specialist | 1/2010 - 1/2012 |
| Mentor Technical Group | Project Manager (Pfizer Caguas Wyeth Pharma) | 1/2007 - 1/2009 |
| Advance Instrument/Aqs | Qa Auditor And Quality Engineer (Bristol Myers Squibb Wyeth Pharma) | 1/2004 - 1/2007 |
| Ipr Pharmaceuticals Inc. | Production Supervisor | 1/1991 - 1/2004 |
| Galephar Inc. | R & D Chemist | 1/1989 - 1/1991 |
| Ayerst/Wyeth Pharmaceuticals Inc. | Senior Chemist | 1/1987 - 1/1989 |
| Roche Products Inc. | Laboratory Analyst | 1/1984 - 1/1987 |
Accomplishments
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