Key Responsibilities
At Sun Pharma, we commit to helping you “
Create your own sunshine
”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Position Summary –
- Implement, operate, monitor and maintain Quality Systems which enable operations on site to occur in an effective manner and in compliance with Global Quality Standards and cGMPs.
- Review and Archival of Quality System documents.
- Follow up for timely closure of Quality Management System documents.
- Participating in the investigation analysis for Deviations, OOS, OOT,
Complaints and Audit finding, moreover responsible for providing batch disposition decision as per the outcome of Deviation, OOS and OOT investigation.
- Supporting in external audits preparations and responding to audit findings.
- Compilation of the Internal audits response and follow up.
- Assist in scheduling and preparation of management review meetings.
- Organize the CAPA meeting, coordinate/manage CAPA efforts and interact with customers to conduct complaint investigations.
- Handling of Change Management & CAPA Management System.
- Assist to author, review and update quality procedures as applicable.
- Responsible for Handling of Complaints, Mock recall/Recall and withdrawal of Drug Products.
- Retentions Sample Management.
- Preparation of APR/PQR.