1. To approve and monitor analysis carried out under contract. 2. To support and lead department during local and international audit. 3. To ensured that necessary testing is carried out. 4. Review of annual product quality. 5. To ensure timely insurance of certificate of analysis for dispatches. 6. Complete day to day activities of Quality Control.
The Plant Head will oversee and manage all aspects of production planning, manufacturing operations, equipment efficiency, and quality & safety compliance in alignment with local FDA and regulatory guidelines. * Develop and implement production plans to meet delivery timelines and ensure product availability as per order requirements. * Review and approve the monthly production plan and oversee its execution. * Ensure all shop floor activities are conducted in strict compliance with cGMP, SOPs, BMR, and FDA guidelines. * Monitor and enforce entry/exit procedures, gowning (primary and secondary), and personnel hygiene practices. * Supervise manufacturing and packaging activities to ensure adherence to laid-down procedures, batch records (BMR/BPR), and SOPs. * Review and authorize plant layouts and operational processes for efficiency and compliance. * Coordinate with the purchase department for timely procurement of raw materials (RM) and packing materials (PM). * Authorize consumable plant indents, including chemicals, equipment, and stationery. * Optimize available resources to achieve process improvements and productivity gains. *Maintain and improve productivity, yield, and equipment efficiency through continuous monitoring and upgrades. * Ensure timely completion of internal, regulatory, and financial audits, adhering to all compliance requirements. * Execute and manage new project activities as assigned by management. * Identify opportunities for process improvement and implement initiatives to enhance overall operational efficiency.
1. Monitoring of RoDTEP Claim. 2. Monitoring of duty Drawback Claim. 3. Monitoring of Advance Authorization application and closure and EPCG Closure. 4. Monitoring of DGFT AND LCEGATE online application 5. Review of RBI Compliance. 6. Co-operating Scrap and discarded solvent sales 7. Freight Audit.
1.Establishment, Implementation and Maintenance of Quality system. 2.Approval of Standard Operating Procedures, Master Batch Manufacturing and Master Batch Packing Records. 3. Authorization of written procedures and other documents including amendments like Master Formula Records, Raw Material specifications, Packing Material specifications, Product specifications & General Analytical Specifications. 4. Monitoring of Compliance with GMP requirements. 5. Review and approval of change control, deviations, Risk assessment, Corrective action Preventive actions and other Quality management system related documents. 6. Inspection, investigation and taking of samples in order to monitor factor that may effect product quality. 7. Organizing Vendor Audit, Approval of new vendor & Vendor Evaluation. 8. Handling of regulatory audits 9. Review and approval of Process validation, cleaning validation, Water validation, HVAC Qualification & other Qualification & validation protocols & reports distribution. 10. Provide training related to GMP including the application and principles of Quality assurance 11. To Comply with the company policies, procedures and quality standards. Co-ordinate with production, quality control, maintenance and stores department for Improving various quality concerned aspects. 12. Review all Quality assurance systems & Regulatory requirements for their current status on regular basis. 13. Responsible for ensuring the quality management system is implemented and maintained in accordance with ISO 9001:2008 requirements & that quality matters are resolved by those holding the relevant responsibility to do so. 14. Preparation of all regulatory documents related to licence application, WHO-GMP certificate and renewal of Licences and GMP certificates. 15. Ensure the regulatory documents like tender applications, performance certificate, general GMP certificate, Production certificate, No conviction certificate, Manufacturing and marketing certificate, etc as per the requirements. 16. Authorization of Reprocess / Rework procedures. 17. Any other responsibility as delegated by Management time to time.
Job description 1. System Service, Installation of system like windows. 2. Roles and Previlegs. 3. Network. 4. Other technical Support Role: IT Support - Other Industry Type: Pharmaceutical & Life Sciences Department: IT & Information Security Employment Type: Full Time, Permanent Role Category: IT Support
We are seeking a dynamic and motivated Product Marketing Specialist to join our team in the Pharmaceutical & Life Sciences industry. The role involves creating and implementing effective marketing strategies, managing product promotions, and collaborating with cross-functional teams to drive brand growth. Candidates must be ready to travel as required to meet business goals. Key Responsibilities: Develop and execute marketing campaigns. Collaborate with sales and product teams to align marketing strategies. Conduct market research to identify opportunities. Qualifications: Relevant experience in marketing or communications.
1. Tender preparation. 2. Bank Grantee / EMD preparation / EMD follow up. 3. Registration of all central/state Govt ,Railways. 4. Sample / NABL/ COA reports. 5. Certificate / CA / Production details / communication letter.