Description
SUMMARY: * More than 5 years of Experience in cGMP regulated environment. * Manage control of changes, Deviations, OOSIR and CAPA * Review batch records and releases lots * Prepare and revise Standard Operating Procedure for cGMP Equipment * Work both independently and in team to finish project on-time. * Knowledge of FDA regulations and 21 CFR 210 & 211, cGMP/GLP/GDP guidelines for solid and liquid drug products.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Cosmetic Essence Innovation | Qa Inspector | 4/2017 - 4/2017 |
| Baroque Pharmaceuticals | Qa Supervisor | 2/2010 - 6/2014 |
| Daywell Pharmaceuticals | Qa Associate | 2/2009 - 2/2010 |
| West Coast Pharmaceuticals | Qa Associate | 7/2008 - 1/2009 |
Education
| SCHOOL | MAJOR | YEAR | DEGREE |
|---|---|---|---|
| Gujarat University | 2008 | Bachelor Degree | |
Accomplishments
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