AstraZeneca is hiring for two high-impact Pharmacovigilance jobs in Bangalore 2026: Japan Local Case Advisor, GBS Patient Safety and Regulatory Review Advisor, Patient Safety. These roles are ideal for life science professionals with experience in ICSR processing, regulatory reporting, and pharmacovigilance compliance.
If you’re looking for AstraZeneca Pharmacovigilance jobs in India, this is a strong opportunity to join a global safety reporting team supporting patient safety operations.
1️⃣ Japan Local Case Advisor – GBS Patient Safety
📍 Location: Bangalore, India
🕒 Full-Time | Career Level C
🗓 Posted: 23 February 2026
Role Overview
The Japan Local Case Advisor will manage Individual Case Safety Reports (ICSRs) for Japan, ensuring compliance with Japanese regulatory requirements and global pharmacovigilance standards. This role requires Japanese language proficiency (N2 or above) and experience in safety database data entry.
Key Responsibilities
- Accept, validate, and assess Japan domestic safety cases
- Perform ICSR data entry with high accuracy
- Conduct preliminary case evaluation and follow-ups
- Ensure compliance with Japanese AE reporting timelines
- Support audits, inspections, and CAPA implementation
- Maintain QMS and safety documentation standards
Essential Qualifications
- Life Science / Pharmacy / Medical degree
- 1–2 years experience in safety database data entry
- Japanese proficiency (N2–N1 preferred)
- Basic pharmacovigilance knowledge
- Experience with ARGUS safety database preferred
2️⃣ Regulatory Review Advisor – Patient Safety
📍 Location: Bangalore, India
🕒 Full-Time | GCL C2
🗓 Posted: 22 February 2026
Role Overview
The Regulatory Review Advisor ensures accurate and timely submission of Adverse Event Reports, Periodic Safety Update Reports (PSURs), and ICSRs to global health authorities. This role focuses on regulatory compliance, inspection readiness, and pharmacovigilance reporting excellence.
3–6 years of pharmacovigilance / regulatory reporting experience
Key Responsibilities
- Prepare and submit regulatory safety reports
- Ensure compliance with Good Pharmacovigilance Practice (GVP)
- Monitor evolving regulatory guidelines
- Review ICSR submissions (E2B format)
- Support audits and regulatory inspections
- Provide internal training on reporting requirements
Essential Qualifications
- Degree in Pharmacy / Medical / Life Sciences
- Experience in regulatory safety reporting
- Knowledge of MedDRA & WHODrug coding
- Experience with Argus / ArisGlobal systems
- Strong documentation & compliance skills
Why Apply for AstraZeneca Pharmacovigilance Jobs?
- Global exposure in safety reporting
- Work with multinational regulatory teams
- Hybrid work model (minimum 3 days office)
- Career growth in regulatory affairs & PV
- Competitive salary & learning opportunities
Salary (Estimated Market Range – Bangalore 2026)
- Japan Local Case Advisor: ₹5.5 – ₹8.5 LPA
- Regulatory Review Advisor: ₹8 – ₹14 LPA
(Salary may vary based on experience and language proficiency.)
How to Apply
Application Link For Japan Local Case Advisor – GBS Patient Safety
Application Link For Regulatory Review Advisor – Patient Safety
