About this role

Plan, conduct, and lead internal corporate quality audits across Sun manufacturing sites.
Audit analytical laboratories, stability and microbiology including R&D Labs. (QC SME)
Review laboratory controls compliance with USP, EP, IP, and other regulatory expectations.
Assess laboratory investigations including OOS, OOT, atypical results, and invalidation practices.
Evaluate data integrity controls within laboratory systems.
Review method validation, transfer, verification, and lifecycle management processes.
.· Conduct follow-up audits to verify CAPA effectiveness
Evaluate computerized systems used in QC laboratories.
Review inspection observations and assess compliance risks.
Support sites during USFDA, MHRA, Health Canada, TGA, ANVISA and other inspections.
Prepare comprehensive audit reports and assess CAPA provided for correctness and completeness
Evaluate audit trail reviews and electronic records management
Track audit observations and CAPA closure timelines.
-. Develop corporate quality metrics and compliance dashboards.
Travel Estimate
Need base
Job Requirements
Educational Qualification
Master of Science

Tenure: Min 18 Years
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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