Opportunity for M. Pharma/ M. Sc as a Quality Assurance Executive at Jubilant Pharmova Ltd – Apply Now

Are you an M. Pharma or M. Sc graduate looking for an exciting career opportunity? Jubilant Pharmova Limited in Nanjangud is seeking a dedicated Quality Assurance Executive to join their team. This prestigious role offers the chance to work with a leading pharmaceutical company, ensuring top-notch quality standards in a dynamic and innovative environment. If you have a passion for excellence and a keen eye for detail, don’t miss this opportunity to advance your career with Jubilant Pharmova Limited.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.

Job Title – Quality Assurance Executive

Qualification for QA Executive at Jubilant Pharmova Limited

Post Graduate in Science/ Master of Pharmacy/ Bachelors of Engineering.

Experience for QA Executive at Jubilant Pharmova Limited

Must have 4+ Years of experience working for an API industry.

Key Responsibilities for QA Executive at Jubilant Pharmova Limited

1. Shall be responsible for quality oversight in Production blocks and shall review process, procedure, facility and training.
2. Batch release (or reject) activity for API’s manufactured at all Plants. This includes review of BPRs, review of IOCBN, verification and distribution of PAF, review of product label and approved label, retaining control sample and verification, inspection as per the checklist for finished product release to customers and updating of finished product distribution records.
3. Review & evaluation of change controls, clean room allocation form, material re-allocation form, reprocess approval form and Packing clearance form and closure of the same before the product release.
4. Responsible for visual inspection and line clearance for the product change over activities.
5. Perform the cleaning validation samples as per approved protocol.
6. Must have knowledge on handling all QMS related activities.
7. Shall be responsible to identify the area of improvement and to review the followings:

• To review training records on the particular operations that the employee performs.
• Plant area & pharma room cleaning is performed as per established procedure.
• Equipment status board are updated with current status.
• Availability of current version of SOP for operation and calibration of equipment in the work Place & accessible to operating personnel.
• Batch production records are placed in work stations during the entire operations.
• Equipment usage and cleaning log is updated by operating personnel.
• Sampling procedure for in-process & intermediate is followed by operating personnel.
• Weighing balance/measuring instruments used in production are calibrated as per established procedure and records are maintained.

• All the accessories (scoops, samplers, scrapper etc.) are coded and cleaned as per established procedure.
• Online monitoring the recording of batch production record & batch cleaning record to comply the ALCOA.
• Dispensing of intermediates and cleaning of dispensing room performed as per established procedure.
• Intermediates, rejected materials are stored in designated place and temperature & relative humidity is maintained.
• Entry & exit procedure available in the clean room & followed by operating personnel during routine operations.
• Equipment are cleaned within the specified time after use as per established procedure.
  Sampling procedure for cleaning samples during product changeover cleaning is followed by operating personnel.
• Monitoring of process & cleaning validations executing as per approved protocol.
• To coordinate for root cause investigation for product failures & customer complaints.
• Coordination and implementation of CAPA for all audit observations & any non-conformances.
• Communicate with management, production regarding questionable measurements, non-conformance issues.
• Shall be responsible for SAP activities.
• Shall be responsible for lifecycle management activities of production
• Shall be responsible for the track wise activities.
• Shall be responsible for initiation & evaluation of CCF, MRF, PCF, CRF & RPF in track wise and SAP.

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