To ensure the qualification and maintenance of department, process, premises and equipment.Responsible for monitoring and control of the Autoclave activity. Batch manufacturing and batch filling activity. Responsible for monitoring and control Required Candidate profile Sterile Injectable Production Experience Qualification- B. Pharma, M. Pharma & M.Sc. To ensure the production incidents and deviations are reported, evaluated, investigated and the conclusions
1.To operate utility related equipment's and maintain documented record according to SOP. 2. To prepare chemical solution for water system and cooling tower. 3. To maintain & record daily monitoring parameters. 4. To carry out filter replacement Required Candidate profile 6. To carry out sanitization of PW S&D and sterilization of WFI S&D system as per frequency. 7. To carry out cleaning of storage tanks and cooling towers as per frequency and maintain good
Planning & Execution of Validation/Qualification activity at site. Execute/ support during Instrument calibration at site Perform equipment validation/ qualification /periodic qualification as per protocols Required Candidate profile Preparation of raw data and reports for executed calibration & validation/ qualification Involve during preparation of equipment validation/ qualification protocols & reports.
Identify for partners / opportunities in distribution of existing products or CMO Develop sales and marketing plan for the countries actively promoted. Forecasting of new orders to supply as per plan. Required Candidate profile Lead generation of new customers and conversion thereof To identify new products to launch in covered markets. To explore new markets for existing products/ New products.
Handles GSTR-1/3B filing, 2A/2B reconciliation, TDS compliance, audit coordination, annual returns, and ensures timely tax filings. Supports GST audits and maintains records per latest tax laws.
Perform chromatographic analyses and tests, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. Required Candidate profile Stay informed about industry trends,advancements in chromatographic technology,regulatory changes related to chromatographic analysis,quality control. Participate in continuing education/training
To ensure the qualification and maintenance of department, process, premises and equipment. Responsible for monitoring and control of the Autoclave activity. Batch manufacturing and batch filling activity. Responsible for monitoring and control Required Candidate profile Sterile Injectable Production Experience. To ensure the production incidents and deviations are reported, evaluated, investigated and the conclusions are recorded, and participate in investigations
Responsible for Monitoring/controlling/Planning/Handling of Manpower of Packing activity along with documentation control and well knowledge of SAP activity.Capable to Preparation of daily report with respect to output and line efficiency. Required Candidate profile Coordination ability with cross functional team.
Responsible for end-to-end customer order supply, production scheduling, MRP preparation, and maintaining GMP documentation. Manages ERP data, generates reports, handles import/export documentation, customs clearance, and claims export incentives.
Should have background of Sterile Formulation /Ophthalmic products Managerial level experience required 10+ years
To lead and manage sterile pharmaceutical manufacturing operations (Ophthalmic / Injectables), ensuring adherence to cGMP, regulatory guidelines, safety standards, and production targets while maintaining high product quality and cost efficiency. Required Candidate profile B. Pharm / M. Pharm / B.sc /M.Sc 15–20 years of strong experience in sterile/injectable manufacturing with at least 10+ years managerial role
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