Ensuring implementation of cGMP practice at site.

- Ensuring readiness of Production, Packaging and Warehouse for regulatory customer and internal Inspection.
- Coordinating with Technical operation team for smooth technology transfer and synthesis of recent products.
- Process validation and continuous process monitoring.
- Follow-up with HR and Admin for manpower and other services.
- Responsible for management of Deviation, investigation, CAPA, Change control, Market Complaint, OOS and OOT
- Implementation of Global CAPA
- Leading Quality Risk Management project at site.
- Leading Quality Communication Program.
- Leading the Cross Contamination project at site
- Ensuring the Data Integrity and GMP compliance at R&D.;
- Handling of Productivity improvement project, Cost saving and safety project.
- Handling of Trouble shooting.
- On Job and Technical Training to R&D; personnel.
- Development of people with respect to technical knowledge, problem solving using right approach..




- Development of quality culture in department by educating risk base approach.
- To ensure effective implementation of quality management systems as per cGMP and international requirements
- Leading the procurement, installation and qualification of New equipment and instruments.
- Review and approval of cleaning validation, cleaning verification protocol and report.
- Review and approval of process validation / Process evaluation / hold time / General study protocol and report.
- Review of the procedures /System to avoid the gap between the procedure vs compliance.
- Review of the risk assessment and to ensure the mitigation plans are implemented.
- Leading Implementation of Manufacturing Execution System (MES ) at site.

Pay: ₹309,966.39 - ₹1,339,403.75 per year

Benefits :

- Health insurance
- Provident Fund

Work Location: In person

📌 Quality Assurance Executive (Hyderabad)
🏢 VIVAN life Sciences
📍 Hyderabad