
Sun Pharma offers affordable, high-quality medicines worldwide through innovative R&D and global manufacturing facilities.
This role is part of Corporate Quality Audits function responsible for conducting Sun site audits to ensure regulatory compliance. The role includes conducting six system-based Quality audits at all manufacturing locations of SUN sites, preparing audit reports, and reviewing responses from sites. Additionally, the role involves coordinating with audit teams and auditees, categorizing non-conformities, and supporting business areas in achieving compliance to regulations and Sun policies/procedures.