6 Job openings found

Job Description: We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle. Key Responsibilities: Perform in-process checks during various stages of API ...

Responsibilities Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations. Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures. Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms. Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing. Support quality investigations and prepare required ...

Monitors the work of manufacturing technicians and quality technicians, manages record keeping, and prepares reports for management Works with software or websites to ensure they run properly by performing manual and automated tests during development Ensures products meet quality standards and industry benchmarks by monitoring processes, inspecting goods and services, and proposing ...

Documentation & Compliance: Maintain accurate and complete laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Prepare and review Certificates of Analysis (CoAs), test reports, and deviation reports. Ensure compliance with company SOPs, safety protocols, and regulatory requirements (e.g., FDA, EPA, ISO). Process Validation & Improvement: Participate in validation of ...

  Operate, monitor, and maintain Compression machines (e.g., Parle Elizabeth – 37 Station & 51 Station). Handle Coating machines (e.g., Gansons – 60 Pan) for tablet coating processes. Manage Capsule filling machines (e.g., Pacifab LLP) ensuring accuracy and compliance. Operate Liquid Filling & Manufacturing equipment (Liquipack) for syrup, suspension, or solution formulations. Run Granulation equipment ...

Prepare and review SOPs; ensure adherence to cGMP and QMS standards. Receive, verify, and record materials from vendors; maintain stock registers and monthly reports. Monitor inventory levels, reconcile discrepancies, and ensure timely stock availability. Coordinate with purchase, QC, and production teams for smooth workflow and batch planning. Oversee dispatches, packing, loading/unloading, and site material ...