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Execute the initiation and/or evaluate deviation(s), interview personnel, analyze root cause, assess impact, identify corrective / preventive actions, present to management and close investigations in the Quality Management System (QMS). Aseptic/Parenteral experience preferred.
In addition, the on-site resources may support the management of the investigation lifecycle documentation and CAPA.
Act as facilitators for the necessary information related to the support of the existing processes and expedite the implementation of Investigation process modifications.
Work on a team under a Senior Manager. Min 5 years’ experience.
Additional Information
| Job Type: | Non IT Job |
|---|---|
| Work Authorization: | Valid Work Visa |
| Employment: | Corp-Corp |
| Functional Area: | Manufacturing |
| No. of Job Openings: | 2 |
| Gender: | Any |
| Qualification: | High School |
| Industry: | Healthcare / Pharma / Bio-tech |
| Language: | English |

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