Qualification: Bsc, B.Pharm, Msc, M.Pharm
Department: Quality Assurance, Quality Control
QA: QA Documentation, QA Validation , IPQA
1. QA Documentation : Technology transfer, SOP preparation, Documentation management ,Training management, Batch records review, management & Artworks management.
2. QA Validation :
- Preparation, review & execution of the equipment qualification i.e. Autoclave validation, Tunnel –validation, Vial / Ampoule washing machine validation, Lyophilizer validation.
- Preparation, review & execution of the utilities qualification i.e. HVAC & LAF validation, Compressed air validation, Nitrogen gas validation, Water system validation.
- Preparation, review & execution of the initial qualification of the equipment / utilities i.e. DQ, IQ,
- OQ & PQ of the equipment / utilities
- Handling of the Process validation.
- Handling of the Cleaning Validation
- Handling of the Media fill activity.
- Handling of the QMS activities i.e. Change control, Deviation, CAPA
- Handling of the Risk Assessment.
3. IPQA :
1. Responsible for line clearance and in process checks for all areas of Small Volume Parenteral
2. Responsible to maintain the document as per cGMP.
3. Ensuring manufacturing practices asper cGMP
4. Conducting shop floor inspection & reporting of the same to the department head
5.Conducting shop floor training of the staff
6. Responsible for initiating Change Control/Deviation/Non-Conformance /Incident / CAPA
7. To assist the Head of Department for preparation of regulatory inspection.
Recording and verification of BMR/ BPR and related activities
8. Executing the validation/revalidation activity of Autoclave / DHS / AHU / Ampoule & Vial Washing Machine
9. Any other responsibilities assigned by the Head of Department
QC Vacancies – QC Executive
Experience : 4- 7 years
Job Responsibilities :
1. Hands on experience on HPLC /GC
2. Handling of instruments like Auto titrator, Uv and IR
3. Wet and Dry analysis.
4. Analysis of Raw materials, Finished Good and other analytical samples
5. Review of RM, FP, Stability, calibration reports.
6. Planning and execution of analytical samples.
7. Investigation of deviation PCC, OOS, Job incident etc.
8.Revision of reports received from CTL, Regulatory compliance.
Interview Date: 3rd December, 2022
Time: 10:00 AM – 3:30 PM
Venue: Sovereign Pharma Pvt. Ltd. | Survey No. 46/1-4, Kadaiya Village | Nani Daman – 396210
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