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.”
Key responsibilities:
- To conduct the audit of Quality Management Systems as per the Corporate Quality Audit program and provide the support for compliance activities across all SUN Pharma Sites.
- To follow the Corporate Quality Policies, Global Quality standards and applicable Regulatory Guidelines.
- To conduct the Quality audit of manufacturing sites of Sun Pharma as per the schedule.
- To inform audit findings to Lead Auditor / HOD and conclude the non-conformity against respective regulatory requirements.
- In case as a lead auditor, coordination with audit team and auditee, compilation of audit findings and review of audit report.
- Categorization of non-conformity into Critical, Major and Minor, appropriately.
- To prepare draft audit report as specified SOP from the last day of audit.
- To raise the change control in case of deviations from the approved audit schedule.
- Attend the training courses, conferences or association meetings to continue to gain knowledge of current industry standard, trend and regulatory agency interpretation of GMP requirements.
- Participate and support project work as allotted by reporting authority.
