Research Associate

4 weeks ago


Sanand Ahmedabad Gujarat, India Auxilla Pharmaceuticals and Research LLP Full time

1. Review of Analytical method development protocols and reports.

2. Review of Analytical method validation protocols and reports.

3. Review of product development report and related documents.

4. Review of technology transfer related documents.

5. Review of SOP, specification, STP, COA and data generated at various departments like AD, FD, WH, EN etc.

6. Review of batch documents.

7. To prepare and review SOP.

8. Review URS, DQ, FAT, IQ, OQ and PQ documents.

9. Responsible for performing area qualification in close liaison with engineers and vendors.

10. Review of instrument/equipment related vendor protocols or in-house protocols and reports to deliver complete package of qualification documents.

11. Ensure timely calibration of Instrument/Equipment as per calibration schedule.

12. Establish and maintain strong relationship with cross functional department.

13. Documentation control.

14. To conduct self inspection.

15. Storage, withdrawal and handling of stability samples as per stability program/protocol.

Any other responsibilities as and when suggested by HOD/management.

**Job Types**: Full-time, Permanent

Pay: ₹15,000.00 - ₹25,000.00 per month

**Benefits**:

- Food provided
- Health insurance
- Leave encashment
- Provident Fund

Schedule:

- Day shift

**Experience**:

- Quality assurance in R&D Center: 1 year (required)

**Location**:

- Sanand, Ahmedabad, Gujarat (preferred)

Work Location: In person

Application Deadline: 17/06/2024


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