Occupation:Not Listed |
Location:Brooklyn, NY |
Education Level:Some College Units Completed |
Will Relocate:YES |
Description
CAREER SUMMARY Quality Assurance Professional with experience in pharmaceutical manufacturing enforcing quality standards in a manufacturing unit. Skilled at studying industry and consumer requirements, running tests, writing quality assurance procedures, preparing quality reports, and assigning quality assurance tasks to employees. Proficient interacting with various departments including Supply Chain, Production, MS&T, Validation, R&D, and Compounding to review, develop and implement production system to improve operation and efficiencies to batch record. Experienced with 21 CFR Part 210, 211 and 21 CRF 211.110 * Certified in Gowning Procedure and Personnel monitoring in Aseptic. * ARS Autoclave machine for the sterilization of all equipment and supplies. * Conducted investigations for Manufacturing and Packaging discrepancies as needed.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Fougera/Sandoz/Novartis Pharma Inc. | Quality Compliance Documentation Sr. Associate | 7/2010 - 6/2017 |
| Nycomed | Documentation Specialist | 5/2008 - 7/2010 |
| P.L. Development | Document Control Coordinator | 3/2008 - 4/2008 |
| Talecris Biotherapeutics | Aseptic Technician Contract | 3/2007 - 4/2008 |
| Pharmaceutical. | Scientist Technician I | 3/2007 - 3/2007 |
| Pfizer Inc. | Quality Assurance Specialist/Aseptic Operator | 3/2007 - 3/2007 |
| Education/Certification Training | New York Institute Of Technology | 3/2007 - 3/2007 |
Accomplishments
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