Posted:1 month ago|
Platform:
On-site
Full Time
Handling of QMS activities (CCF, Deviations and OOS etc.) Preparation and review of SOPs, EOPs, OCPs, BMR and production related documents. Review of batch reports and Involvements on productivity improvements and batch failure investigations. Preparation of AIM and HIRA register. Preparation of HAZOP study. To coordinate with QA for all the validation, qualification, and Audit preparedness. Adherence to Standard Operating Procedures, product specifications. Adherence to Good manufacturing Practices and Good Documentation Practices. Review All completed documents and ensuring that completeness and signed. Data entry in Quality records. Qualification: BSc / MSc Experience: 3 - 4 years Show more Show less
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Visakhapatnam, Andhra Pradesh, India
Experience: Not specified
Salary: Not disclosed
Visakhapatnam, Andhra Pradesh, India
Experience: Not specified
Salary: Not disclosed
