QA Job at Jubilant Pharmova Limited – MPharma Apply Online
The Position
Organization: Jubilant Pharmova Limited
Designation: Officer – QA
Location: Nanjangud, Mysore
Key Responsibilities
Quality Oversight:
- Responsible for quality oversight in production blocks and reviewing process, procedures, facility, and training.
Batch Release:
- Batch release (or rejection) activity for APIs manufactured at all plants, including:
- Review of BPRs.
- Review of IOCBN.
- Verification and distribution of PAF.
- Review of product labels and approved labels.
- Retaining control samples and verification.
- Inspection as per the checklist for finished product release to customers.
- Updating finished product distribution records.
Review & Evaluation:
- Change controls.
- Clean room allocation forms.
- Material re-allocation forms.
- Reprocess approval forms.
- Packing clearance forms and their closure before product release.
Additional Responsibilities:
- Visual inspection and line clearance for product changeover activities.
- Performing cleaning validation samples as per approved protocol.
- Handling all QMS-related activities.
Improvement and Review Areas:
- Reviewing training records on specific operations performed by employees.
- Ensuring plant areas and pharma rooms are cleaned as per established procedures.
- Verifying that equipment status boards are updated with current statuses.
- Checking the availability of the current version of SOPs for operations and calibration of equipment.
- Ensuring batch production records are placed in workstations during operations.
- Monitoring equipment usage and cleaning logs updated by operating personnel.
- Following sampling procedures for in-process and intermediate operations.
- Verifying that weighing balances/measuring instruments are calibrated and records maintained.
- Ensuring accessories (scoops, samplers, scrappers, etc.) are coded and cleaned as per procedures.
- Monitoring online recording of batch production records and cleaning records to comply with ALCOA.
- Overseeing dispensing of intermediates and cleaning of dispensing rooms as per procedures.
- Ensuring intermediates and rejected materials are stored in designated places with temperature and relative humidity maintained.
- Confirming entry and exit procedures in clean rooms are followed by personnel.
- Verifying equipment is cleaned within the specified time after use as per procedures.
- Ensuring sampling procedures during product changeover cleaning are followed.
- Monitoring process and cleaning validations executed as per approved protocols.
Coordination and Communication:
- Coordinating root cause investigations for product failures and customer complaints.
- Implementing CAPA for audit observations and non-conformances.
- Communicating with management and production regarding questionable measurements and non-conformance issues.
Other Responsibilities:
- Handling SAP activities.
- Managing lifecycle activities in production.
- Handling track-wise activities.
- Initiating and evaluating CCF, MRF, PCF, CRF, and RPF in track-wise and SAP.
Person Profile
- Education Qualification: Postgraduate in Science/Master of Pharmacy/Bachelor of Engineering.
- Experience Range: 1+ years.
Link to apply: APPLY ONLINE HERE
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