Posted:6 days ago|
Platform:
Work from Office
Full Time
1. Preparing and implementing of standard operating Procedures, Batch records, Protocols, cleaning procedures and relevant log sheets.
2. Maintaining documents as per regulatory and cGMP norms.
3. Handling of QMS activities, Change controls, Deviations, Incidents and risk assessments.
4. Responsible for ensuring the department employees for training as per training plan schedule in the TRIMS.
5. Responsible to attend all training programs, SOPs and cGMP trainings relevant to area and equipments.
6. Responsible for monitoring of periodic review of SOP’s related to FP Departments and ensuring the completion with in due date.
7. Performing DQ, IQ, OQ, and PQ for the equipment’s.
8. Writing of relevant Batch documents and log books.
9. Execution of production plan for formulation and filling.
10. Achieving planned FP targets with strict adherence to cGMP.
11. Execution of planned activities of Aseptic Processing Areas like media fills simulation trials,
Formulation and filling activities.
12. Execution of preventive maintenance plan for equipment’s in coordination with Engineering and QA departments.
13. Performing day to day activities as per requirements.
14. Reporting all the activities, deviations and issues to Reporting officer.
ITI/ DIPLOMA/ B. TECH/ Pharmacy With Relevant experience
Hetero
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