56 Job openings found

Lead and manage the complete Quality Control laboratory operations. Supervise QC testing of Raw Materials, Packaging Materials, In-Process Samples, Finished Products and Stability Samples. Ensure analytical testing is performed as per approved specifications, STPs, pharmacopoeial and regulatory requirements. Manage analytical instruments such as HPLC, GC, UV, FTIR, Dissolution, KF, pH Meter, TOC and ...

Job Responsibilities (Universal Chemicals) Ensure all products meet quality standards and specifications. Perform in-process and final product quality checks. Review and maintain QA documents, records, and reports. Prepare and update SOPs, specifications, and quality documents. Monitor GMP, safety, and quality compliance in the plant. Handle deviations, CAPA, and change control activities. Participate in internal and external quality ...

Key Responsibilities: Perform analysis of Raw Materials (RM), In-Process Samples, Finished Products (FP), and Stability Samples. Operate analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, and Dissolution Apparatus. Prepare and standardize reagents, solutions, and reference standards. Maintain analytical records, laboratory notebooks, and test reports as per cGMP and GLP requirements. Perform calibration and routine ...

Job Responsibilities (Universal Chemicals) Ensure all products meet quality standards and specifications. Perform in-process and final product quality checks. Review and maintain QA documents, records, and reports. Prepare and update SOPs, specifications, and quality documents. Monitor GMP, safety, and quality compliance in the plant. Handle deviations, CAPA, and change control activities. Participate in internal and external quality ...

Responsibilities To Receive the Raw material and Packing material as per standard operating procedure.  To Prepare Goods arrival report (GAR), intimation to Quality Control Lab for Raw material sampling.  To ensure daily calibration and verification of electronic weighing balance.  To issue of material to production as per standard ...

  Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Perform line clearance and in-process checks. Ensure compliance with cGMP, GDP, and SOP requirements. Handle deviations, change control, CAPA, OOS, and OOT investigations. Prepare, review, and update SOPs and QA documents. Conduct GMP audits and shop floor inspections. Monitor documentation and maintain data integrity. Coordinate with Production, ...

Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable). Review and approve analytical results, COAs, test reports, and raw data. Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.). Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.). Review and update SOPs, STPs, GTPs, ...

Key Responsibilities Operate tablet coating machines such as Auto Coater / Conventional Coating Machines. Perform machine setup, startup, operation, and shutdown activities. Check coating parameters including: Spray rate Inlet / outlet temperature Pan speed Atomization pressure Prepare coating solution as per BMR (Batch Manufacturing Record). Monitor coating process and ensure uniform coating quality. Handle loading and unloading of tablets safely. Maintain ...

Responsible for Checking & distribution of approved artwork. Responsible for colour approval of the shade card. Responsible for the Allocation & Verification of the Pharma code. Responsible for the Allocation & Verification of GTIN numbers as per GS1 guidelines. Artwork management as per the product brief. To verify artwork as per the Labelling Act. To review ...

🔧 Key Responsibilities Operate and monitor Blister Packing Machines (Alu-Alu / Alu-PVC). Perform machine setup, changeover, and format adjustments as per production plan. Ensure proper feeding of materials like PVC, Aluminum foil, and printed foils. Conduct in-process checks and maintain batch records as per SOP. Ensure compliance with cGMP, safety, and quality standards. Troubleshoot minor mechanical ...