Drafting and Review of Investigation Reports in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D;, QC and AR&D; etc.
Preparation of Quality Risk Assessment and its Impact Assessment Reports as or when required.
Handling of documents related to Quality Management System (QMS) like Change controls, Deviations, Planned changes, CAPAs etc., as per requirement in co-ordination with cross functional departments like Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D;, QC, AR&D; etc.
Follow the cGMP compliance by following the SOPs and approved procedures.
Responsible for any activities assigned by HOD or Senior Management.
📌 Asst Manager Documentation Investigations Production Api Bidar
🏢 Sai Life Sciences
📍 Bidar
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