Roles and Responsibilities :

- Develop and maintain accurate documentation of BMR (Batch Manufacturing Record) for pharmaceutical products.

- Ensure compliance with QMS (Quality Management System) requirements by implementing change controls, deviations, CAPA (Corrective Action Preventive Action), SOPs (Standard Operating Procedures), and MDDM (Manufacturing Deviation Documentation).

- Collaborate with cross-functional teams to resolve issues related to product quality, manufacturing processes, and regulatory compliance.

- Conduct investigations into non-conformities and implement corrective actions to prevent recurrence.

Job Requirements :

- 3-8 years of experience in a similar role within the pharmaceutical industry.

- Robust understanding of BOM (Bill of Materials), Change Control procedures, CAPA implementation, Deviation investigation techniques.

- Proficiency in using SAP systems or other relevant software tools such as MDM (Master Data Management).

📌 Senior Documentation Executive (Killa-pardi)
🏢 Schott Poonawalla
📍 Killa-pardi