Responsible for monitoring & compliance of Self-Inspection and Quality Audits conducted at site.
Monitoring, review & execution of Technology Transfer activities.
Responsible for the preparation & monitoring of HACCP & its related activity.
Handling of QMS activity.
Handling of Food safety related activities.
Responsible for execution & monitoring of training.
Monitoring & maintenance of EM trends & its reports.
Maintenance & monitoring of SMF, Quality Manual & MLDs.
Preparation, control, archival and review GMP and Quality Documents and recording of the same that includes;
CQPs & SOP's
Protocol and Reports
Logs and Log Books
Monitoring and review of Reprocess and Recovery in manufacturing areas.
Responsible for GMP Compliance in Plant on day to day basis.
Monitoring and controlling activities in areas of Manufacturing, Packing, Labeling and Holding of products shall include;
Review & approval of Batch Documents
Review & approval of Deviations
Review of OOS in Batch
Investigation of Complaints
Review of Change implementation
Review of approval of Nonconformities & rejections
Conducting, Monitoring and controlling activities related to manufacturing process and testing process shall include, Continuous Process Verification
Planning and conducting the Qualification and validation activities that are relevant to manufacturing and testing of products and shall include;
Building and Facility
Salary: INR 4,00,000 - 5,00,000 P.A.
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: R&D
Role: Bio/Pharma Informatics-Associate/Scientist
Employment Type: Permanent Job, Full Time