Unichem Laboratories is hiring experienced Pharmacovigilance professionals for the role of Officer โ Pharmacovigilance Quality & Literature Review at its Mumbai location. Candidates with experience in Argus Database, literature review, aggregate report preparation, and global pharmacovigilance activities are encouraged to apply.
This is an excellent opportunity for B.Pharm and M.Pharm graduates looking for Pharmacovigilance jobs in Mumbai with exposure to global safety operations, literature screening, quality review, EudraVigilance screening, and regulatory submissions.
Unichem Laboratories PV Job Overview
| Job Details | Information |
|---|---|
| Job Title | Officer โ Pharmacovigilance โ Quality & Literature Review |
| Company | Unichem Laboratories |
| Location | Mumbai (Kandivali) |
| Experience Required | 2โ5 Years |
| Qualification | B.Pharm, M.Pharm |
| Employment Type | Full Time |
| Department | Pharmacovigilance / Research & Development |
| Salary Estimate | โน4.5 โ โน7.5 LPA |
| Posted On | May 27, 2026 |
Pharmacovigilance Officer Job Description
Unichem Laboratories is seeking skilled Pharmacovigilance professionals to support global PV operations, literature review, quality management, and safety reporting activities. The selected candidate will work closely with internal teams, regulatory authorities, QPPV offices, and business partners to ensure compliance with global pharmacovigilance guidelines.
Candidates with strong knowledge of GVP modules, Argus safety database, aggregate report preparation, and global submissions will have an advantage.
Key Responsibilities
The selected candidate will be responsible for:
- Supporting Pharmacovigilance (PV) activities across global operations
- Performing literature screening and maintaining literature search records
- Reviewing literature articles for medical and regulatory validity
- Conducting triage and booking in Argus Database
- Completing data entry and quality review in Argus
- Performing EudraVigilance ICSR screening
- Preparing and submitting aggregate safety reports including PADERs
- Developing and maintaining SOPs and Work Instructions (WIs)
- Conducting Pharmacovigilance training sessions for teams and stakeholders
- Managing global safety submissions
- Handling reconciliation activities with QPPV, distributors, and partners
- Supporting case processing oversight activities
- Responding to pharmacovigilance-related compliance queries
Required Qualifications
Educational Qualification
- B.Pharm
- M.Pharm
Experience
- 2 to 5 years of Pharmacovigilance experience
Desired Skills
- Good knowledge of GVP modules and pharmacovigilance guidelines
- Hands-on experience with Argus Database
- Literature review and literature screening experience
- Knowledge of aggregate report preparation
- Understanding of EudraVigilance screening
- Good communication and documentation skills
- Basic computer proficiency
Why Join Unichem Laboratories?
Unichem Laboratories Careers offers professionals an opportunity to work in a regulated pharmaceutical environment with exposure to global Pharmacovigilance systems and compliance processes.
Employee Benefits
- Exposure to global Pharmacovigilance operations
- Experience with regulatory submissions and aggregate reports
- Career growth in drug safety and PV quality
- Opportunity to work with global stakeholders and QPPV teams
- Stable pharmaceutical industry career path
How to Apply
