Jubilant Pharma Limited, a globally integrated pharmaceutical powerhouse, is seeking a talented Executive – Pharmacovigilance to join their dynamic team. If you are passionate about drug safety and regulatory compliance, this opportunity in Greater Noida, Uttar Pradesh, offers you a chance to contribute to impactful healthcare solutions. Pharmacovigilance Jobs in Noida & delhi
About Jubilant Pharma Limited
Jubilant Pharma Limited is a leading pharmaceutical company, recognized worldwide for its innovative approach to healthcare. The company operates in two major segments:
- Specialty Pharmaceuticals – Including radiopharmaceuticals, contract manufacturing of sterile injectables, and allergy therapy products.
- Generics & APIs – Offering solid dosage formulations and active pharmaceutical ingredients.
With state-of-the-art manufacturing facilities in Mysore and Roorkee, Jubilant Pharma ensures high-quality production that meets global regulatory standards such as USFDA, UK MHRA, TGA, PMDA Japan, and others.
Responsibilities in the Role
As an Executive – Pharmacovigilance, you will play a pivotal role in ensuring the safety and efficacy of pharmaceutical products. Key responsibilities include:
- Monitoring and managing adverse drug reactions (ADRs) and preparing regulatory safety reports.
- Ensuring compliance with local and international pharmacovigilance regulations.
- Collaborating with cross-functional teams including R&D, manufacturing, and regulatory affairs to enhance drug safety measures.
- Maintaining and updating pharmacovigilance databases.
- Conducting regular audits and ensuring adherence to Good Pharmacovigilance Practices (GVP).
- Liaising with regulatory bodies and preparing documentation for product safety reviews.
Qualifications
To excel in this role, candidates should meet the following qualifications:
- A degree in Pharmacy, Medicine, or Life Sciences (B.Pharm/M.Pharm) or an equivalent qualification.
- Minimum of 2-4 years of experience in pharmacovigilance or a related field.
- Familiarity with global regulatory guidelines such as ICH, FDA, EMA, and WHO standards.
Key Skills
Successful candidates should demonstrate:
- Strong analytical and problem-solving skills.
- Proficiency in pharmacovigilance tools and databases.
- Excellent communication and teamwork abilities.
- Attention to detail and ability to manage complex data.
- In-depth knowledge of drug safety regulations and compliance standards.
