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 cooperative 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 efficient 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.