Work from Office
Full Time
1) Engineering daily round and document verification in order to compliance.
2) Verification of Calibration planner, preventive maintenance planner to ensure activity done as per scheduled plan.
3) GPS clock time verification across the plant as per schedule, Alarm verification of equipment as per planner.
4) Audit trail verification of equipment (Drug product & Engineering area).
5) Review of memo in system and ensure closure in time with coordination to cross functional team with proper evaluation.
6) Preparation / review of Media fill protocol and report.
7) Preparation of process / cleaning validation protocol & report.
8) Review of cross functional documents (SOP, Validation protocol / report, Study protocol / report etc.)
9) Review and evaluation of QMS documents (Change control, Deviation, Incident etc.
10) Verification and review of Qualification/ Validation activities.
11) Co-ordinate with the cross functional departments as and when required.
12) Any other work allocated by Department Head.
Intas
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