Torrent Pharmaceuticals
Pharmacovigilance Executive
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Ahmedabad, Gujarat, India
Work mode:
Onsite
Published on:
20 August 2026
What they need
Role & responsibilities
- Maintaining Standard Operating Procedures-SOP with Global PV system
- Preparation, review of PV SOPs and work instructions
- Complete ICSR (spontaneous, literature, regulatory and clinical trials) processing, QC and submission
- Preparation of PSUR, RMP and REMS
- Preparation of signal detection report and trend analysis
- Handling of regulatory authority queries and customer complaints
- Preparation of PI, MG, PIL, SmPC and CCDS
- Literature search, review and screening of ICSR and safety studies
- SDEA establishment and compliance check
- Product complaint handling, review and tracking
- Global AER database development, validation and revision
Preferred candidate profile
Candidate with 2 - 7 Years of relevant experience
Interested candidates are requested to share their CVs on [email protected] / [email protected]
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