Senior Officer/Executive (South Goa)

Job Overview: We are looking for a detail-oriented and compliance-focused qualified for the role of Dispatch QA Executive / Officer. The candidate will be responsible for batch record review, batch release support, documentation control, customer documentation coordination, and ensuring adherence to cGMP and quality systems within the plant. The role also involves handling QA activities in a PAS|X MES environment, including workflow approvals, batch record review, exception handling, system coordination, and support for manufacturing and dispatch-related activities. Key Responsibilities
- Ensure adherence to cGMP requirements and approved quality systems within the plant.
- Review executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs), including online review of batch records.
- Support batch release activities and ensure compliance of batch-related documentation prior to release and dispatch.
- Issue batch records, additional pages, formats, and controlled documents as required.
- Handle document sharing with customers and respond to customer queries related to QA documentation and compliance.
- Manage execution, review, and workflow approvals of Shop Floor Orders within PAS|X MES environment.
- Perform batch master verification, review batch record reports, calibration logs, exception reports, and related system functionalities.
- Record and verify in-process sample results and handle direct stock creation/takeout activities within PAS|X system.
- Coordinate label handling and related documentation activities within PAS|X environment.
- Maintain proper documentation practices, record management, and compliance with data integrity requirements.
- Coordinate with Production, QC, Warehouse, and cross-functional teams for smooth execution of QA and dispatch activities.
- Support investigations, compliance activities, and any other responsibilities assigned by the Quality Assurance Manager. Required Candidate Profile
- B.Pharm / M.Pharm / B.Sc. / M.Sc. or equivalent qualification.
- Minimum 5 years experience in Dispatch
- QA within the pharmaceutical manufacturing environment.
- Good understanding of Batch Release, BMR/BPR review, documentation control, and cGMP requirements.
- Exposure to PAS|X MES or similar electronic batch record systems preferred.
- Good coordination, documentation, and compliance management skills. Apply on Kit Job: kitjob.in/job/4m4ak7