Jubilant Pharma has announced a new hiring opportunity for the position of Executive – Pharmacovigilance at its Greater Noida, Uttar Pradesh location. This full-time opportunity is ideal for professionals with experience in pharmacovigilance, drug safety, clinical research, medical writing, regulatory affairs, and case processing.
As one of India’s leading pharmaceutical organizations with a strong global presence in APIs, specialty pharmaceuticals, sterile injectables, and generics, Jubilant Pharma offers an excellent career path for professionals looking to grow in drug safety and regulatory sciences.
If you are searching for Pharmacovigilance Jobs in Greater Noida, Drug Safety Executive Jobs, or Jubilant Pharma Careers 2026, this opportunity deserves your attention.
Jubilant Pharma Limited is a globally recognized pharmaceutical company operating across more than 100 countries. The company specializes in:
- Specialty Pharmaceuticals
- Radiopharmaceuticals
- Sterile Injectable Manufacturing
- Allergy Therapy Products
- Active Pharmaceutical Ingredients (APIs)
- Generic Medicines
- Contract Manufacturing
Its subsidiary, Jubilant Generics Limited (JGL), operates advanced Research & Development centers in Noida and Mysore along with USFDA-approved manufacturing facilities at Mysore and Roorkee.
The organization is known for maintaining high-quality manufacturing standards and regulatory compliance with authorities including:
- USFDA
- UK MHRA
- Japan PMDA
- WHO
- TGA Australia
- Brazil ANVISA
- EMEA
| Particular | Details |
|---|---|
| Position | Executive – Pharmacovigilance |
| Company | Jubilant Generics Limited (Jubilant Pharma) |
| Department | Pharmacovigilance |
| Job Type | Full-Time |
| Location | Greater Noida, Uttar Pradesh |
| Experience | 3–8 Years |
| Industry | Pharmaceutical |
| Date Posted | 29 June 2026 |
The selected Executive – Pharmacovigilance will be responsible for:
- Processing Individual Case Safety Reports (ICSRs)
- Performing pharmacovigilance case assessments
- Preparing accurate medical narratives
- Ensuring compliance with global pharmacovigilance regulations
- Supporting aggregate safety reporting activities
- Maintaining drug safety databases
- Reviewing adverse event reports
- Collaborating with cross-functional medical and regulatory teams
- Supporting quality assurance activities
- Following ICH-GCP and global regulatory guidelines
- Participating in signal detection and safety surveillance activities
- Ensuring timely submission of safety reports
Candidates should possess one or more of the following qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Other relevant Life Science qualifications
Relevant experience in Pharmacovigilance or Drug Safety is preferred.
Jubilant Pharma is looking for professionals with experience in:
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- Argus Safety Database
- MedDRA Coding
- Clinical Research
- Clinical Data Management
- Regulatory Affairs
- Medical Writing
- Case Processing
- ICH Guidelines
- Quality Assurance
- Clinical Trials
- Healthcare Documentation
Knowledge of the following tools is considered an added advantage:
- Argus
- MedDRA
- Python
- Java
- AWS
- Microsoft Azure
- Docker
- GCP
Working with Jubilant Pharma offers several career advantages:
- Global pharmaceutical organization
- Exposure to international pharmacovigilance projects
- USFDA-approved manufacturing ecosystem
- Strong R&D environment
- Career growth opportunities
- Cross-functional learning
- Stable long-term career
- Global regulatory exposure
- Professional development programs
- Competitive compensation package
Although the company has not officially disclosed the compensation, professionals with 3–8 years of pharmacovigilance experience can generally expect:
Estimated Salary: ₹7 LPA – ₹13 LPA
Actual salary depends upon experience, technical expertise, and interview performance.
Greater Noida, Uttar Pradesh, India
