To Co-ordinate with all Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D;, QC, AR&D; for closure of QMS like CAPAs, Investigations”, Deviations in set time as per SOP.
Preparation of “Risk Assessment” and Impact Assessment report as per requirement.
To Co-ordinate with all Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D;, QC, AR&D; for initiation of QMS like CAPAs, Deviations as per requirement.
Follow the cGMP compliance by following the SOPs and approved procedures.
Responsible for any activities assigned by Manager.
📌 Production Documentation//bidar//api Assistant Manager
🏢 Sai Life Sciences
📍 Bidar
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