Production Documentation//Bidar//API

2 weeks ago


Bidar, India Sai Life Sciences Full time

1. 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. 2. Preparation of “Risk Assessment” and Impact Assessment report as per requirement. 3. 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. 4. Follow the cGMP compliance by following the SOPs and approved procedures. 5. Responsible for any activities assigned by Manager.



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