Pharmacovigilance Executive Jobs: Jubilant Pharma is Hiring – Apply Now
Step into the world of global drug safety with Jubilant Pharma Limited, a leading integrated pharmaceutical company. The Executive – Pharmacovigilance role offers an incredible opportunity to work with advanced safety systems like ARGUS while ensuring compliance with global pharmacovigilance regulations. This position is ideal for professionals passionate about drug safety, data accuracy, and regulatory excellence, contributing to one of the most trusted pharmaceutical brands worldwide.
Job Details:
- Job Title: Executive – Pharmacovigilance
- Location: Greater Noida, Uttar Pradesh
About the Company:
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a diverse range of products and services across geographies. The company operates through two key segments: Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL), a wholly-owned subsidiary, manages R&D units in Noida and Mysore, along with two manufacturing facilities in Mysore, Karnataka and Roorkee, Uttarakhand. These facilities are USFDA-approved and focus on manufacturing APIs and dosage forms, catering to worldwide markets. The Mysore site, spanning 69 acres, focuses on lifestyle-driven therapeutic areas such as Cardiovascular (CVS) and Central Nervous System (CNS) disorders. The Roorkee facility caters to a B2B model for EU, Canada, and emerging markets, and holds certifications from major global regulatory authorities including USFDA, PMDA (Japan), UK MHRA, TGA, WHO, and ANVISA (Brazil). Supported by over 500 R&D professionals, JGL develops innovative products across APIs, oral solids, injectables, creams, and liquids. Its in-house BA/BE facility is globally accredited (USFDA, ANVISA, EMEA, etc.), ensuring high-quality standards in research and product development. The Regulatory Affairs & IPR divisions strengthen Jubilant’s competitive edge through patents and global filings.
Education:
Key Responsibilities:
- Perform case processing and data entry activities in the ARGUS Safety database following data entry conventions and timelines.
- Download, triage, upload, and book-in regulatory and EMA MLM ICSR reports.
- Manage literature reports including triaging and book-in.
- Ensure accurate PV-MedDRA coding for adverse reactions.
- Maintain clear and compliant pharmacovigilance documentation following company SOPs and regulatory guidelines.
- Communicate effectively with internal and external stakeholders in a timely manner.
- Stay updated on global pharmacovigilance legislation to ensure ongoing compliance.
- Contribute to aggregate report preparation, signal detection, and regulatory submissions following company SOPs.
