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Sovereign Pharma Pvt. Ltd – Walk-In Interviews for QA / QC on 3rd Dec’ 2022

Sovereign Pharma is a part of Dadachanji Group companies and is a quality-focused and WHO-GMP Geneva certified manufacturing facility for terminally sterilized and aseptically filled injectables, Sovereign Pharma was established in Daman in the year 2003 as a Contract Manufacturing Organization (CMO), supplying quality products to companies worldwide. With a production capacity of around 350 million pieces per annum, Sovereign Pharma manufactures and sells over 1 billion injection doses annually.

Sovereign Pharma Daman | Walk-In Interview- QA / QC | 3rd Dec-22

QA Vacancies – IPQA , DMS , Validation | Injectables | Daman location

1) QA Documentation : Technology transfer ; SOP preparation and management ; Documentation management ; Training management ; Batch records review management & Artworks management

2) QA Validation :

1. – Preparation, review & execution of the equipment qualification i.e. Autoclave validation, Tunnel –validation, Vial / Ampoule washing machine validation, Lyophilizer validation.
2. – Preparation, review & execution of the utilities qualification i.e. HVAC & LAF validation, Compressed air validation, Nitrogen gas validation, Water system validation.
3. – Preparation, review & execution of the initial qualification of the equipment / utilities i.e. DQ, IQ,
   OQ & PQ of the equipment / utilities
4. – Handling of the Process validation.
5. – Handling of the Cleaning Validation
6. – Handling of the Media fill activity.
7. – Handling of the QMS activities i.e. Change control, Deviation, CAPA
8. – Handling of the Risk Assessment.

3) IPQA :

• Responsible for line clearance and in process checks for all areas of Small Volume Parenteral
• Responsible to maintain the document as per cGMP.
• Ensuring manufacturing practices asper cGMP
• Conducting shop floor inspection & reporting of the same to the department head
• Conducting shop floor training of the staff
• Responsible for initiating Change Control/Deviation/Non-Conformance /Incident / CAPA
• To assist the Head of Department for preparation of regulatory inspection.
• Recording and verification of BMR/ BPR and related activities
• xecuting the validation/revalidation activity of Autoclave / DHS / AHU / Ampoule & Vial Washing Machine
• Any other responsibilities assigned by the Head of Department

QC Vacancies – QC Executive

No – 1

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