Sun Pharma Hiring M Pharma Graduates | Apply for Executive QA Pharmacovigilance Role
Sun Pharmaceutical Industries Ltd, a global leader in pharmaceuticals, is hiring an Executive – QA Pharmacovigilance at its Gurgaon office. This role is ideal for candidates passionate about quality assurance within pharmacovigilance systems. As part of the R&D Quality (GPvP QA) department, you’ll play a key role in auditing, compliance management, CAPA tracking, and supporting corporate pharmacovigilance operations.
- Job Position: Executive QA Pharmacovigilance
- Department: R&D Quality (GPvP QA)
- Job Location: Gurgaon – Office
About the Company
Sun Pharmaceutical Industries Ltd is one of the world’s largest specialty generic pharmaceutical companies, delivering high-quality, affordable medicines trusted by healthcare professionals and patients in over 100 countries. Sun Pharma’s R&D Quality (GPvP QA) division is dedicated to maintaining global standards in pharmacovigilance, ensuring product safety and compliance with international regulations.
Job Description
The Executive – QA Pharmacovigilance will assist in developing and maintaining Sun Pharma’s global pharmacovigilance auditing program. The role includes conducting and reporting audits for outsourced parties (CROs, vendors, affiliates, and partners), managing internal audit observation databases, ensuring the implementation of CAPAs, and supporting compliance across all pharmacovigilance activities.
Key Responsibilities
- Assist in developing the global pharmacovigilance system auditing program.
- Conduct and report audits for CROs, service providers, vendors, affiliates, and partners.
- Audit Sun Pharma sites involved in pharmacovigilance activities to ensure compliance with quality systems.
- Manage the Internal Audit Observation Database (IAOD) and share audit and CAPA reports globally.
- Ensure CAPAs are adequately addressed and closed within the stipulated timelines.
- Review and close deviations at global and regional levels to ensure CAPA adequacy.
- Review pharmacovigilance SOPs for completeness, clarity, and compliance with global regulations.
- Prepare and review departmental SOPs to align with company and regulatory standards.
- Assist in the preparation of monthly reports.
- Manage training and records of the GPvP-QA team through the Learning Management System (LMS).
- Support the operations team during corporate and external audits.
- Collaborate with cross-functional teams to maintain quality standards across all pharmacovigilance operations.
- Lead the assessment and tracking of global actions arising from corporate initiatives.
- Perform additional responsibilities as assigned related to R&D quality systems.
- Maintain accurate documentation and records in compliance with quality and regulatory standards.
Educational Qualification
Post Graduate in Pharmacy (M Pharma)
Experience and Skills
- Approximately 2 years of experience in Pharmacovigilance Quality Assurance or PSUR/Signal Management.
- Strong auditing skills and regulatory understanding.
- Excellent attention to detail and accuracy in documentation.
- Good spoken and written English communication.
- Strong interpersonal and liaising skills with cross-functional teams.
