Executive – Pharmacovigilance – India
Job Type: Full-Time, Permanent
Location: India (specific location flexible based on operations)
About Jubilant Pharma Limited:
Jubilant Pharma Limited is a leading global integrated pharmaceutical company, delivering a wide range of pharmaceutical products and services across geographies. The organization operates through two primary business segments:
Specialty Pharmaceuticals – including Radiopharmaceuticals, Contract Manufacturing of Sterile Injectables, Non-Sterile & Allergy Therapy Products.
Generics & APIs – comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients (APIs).
Jubilant Generics Limited (JGL), a wholly-owned subsidiary, has R&D centers in Noida and Mysore and state-of-the-art manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand. Both facilities are globally accredited, including approvals from USFDA, Japan PMDA, UK MHRA, TGA, WHO, Brazil ANVISA, and adhere to international quality standards.
About the Role:
We are seeking an Executive – Pharmacovigilance to support our global operations in monitoring, evaluating, and reporting safety data associated with pharmaceuticals. This role is critical in ensuring patient safety, regulatory compliance, and adherence to global pharmacovigilance guidelines.
Key Responsibilities:
Collect, review, and document adverse events (AEs) and adverse drug reactions (ADRs) from clinical trials, post-marketing studies, and spontaneous reports.
Perform case assessment, triage, and follow-up, ensuring completeness and accuracy of safety data.
Ensure compliance with global pharmacovigilance regulations including ICH-GCP, FDA, EMA, and local regulatory guidelines.
Maintain safety databases and tracking systems, ensuring timely data entry and reporting.
Prepare and submit Regulatory Safety Reports (e.g., SUSARs, PSURs, DSURs) as per regional and global requirements.
Collaborate with cross-functional teams including Clinical Operations, Regulatory Affairs, and Medical Affairs to ensure pharmacovigilance compliance.
Contribute to safety signal detection, risk assessment, and risk management activities.
Support audits and inspections by providing accurate safety documentation and process compliance.
Required Qualifications and Experience:
Bachelor’s degree in Pharmacy, Life Sciences, or a related field.
1–3 years of experience in pharmacovigilance, drug safety, clinical research, or regulatory affairs.
Knowledge of global pharmacovigilance regulations and drug safety processes.
Strong analytical and documentation skills with attention to detail.
Excellent communication skills (verbal and written) in English.
Proficiency in safety databases and MS Office tools.
Preferred Qualifications:
Master’s degree in Pharmacy, Life Sciences, or related discipline.
Experience in regulatory submissions, signal detection, or risk management.
Familiarity with pharmacovigilance tools such as Argus, Arisg, or similar safety databases.
Why Join Jubilant Pharma:
Work in a global pharmaceutical environment with exposure to multiple therapeutic areas including CVS, CNS, and lifestyle-driven treatments.
Be part of innovative R&D projects in APIs, sterile injectables, solid dosage forms, and advanced formulations.
Opportunities for professional growth in a globally accredited organization with a strong commitment to quality and compliance.
Contribute to patient safety and regulatory excellence on an international scale.
Job Category: Pharmacovigilance / Drug Safety / Regulatory Affairs / Life Sciences
About the Organization:
For more details on Jubilant Pharma and its global operations, visit www.jubilantpharma.com.
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