QPS Bioserve India is hiring experienced Pharmacovigilance professionals for multiple Drug Safety Associate and Pharmacovigilance Associate positions in Hyderabad. Candidates with 3โ10 years of experience in ICSR management, regulatory reporting, E2B submissions, and pharmacovigilance operations are encouraged to apply.
This latest Pharmacovigilance job in Hyderabad is ideal for candidates with expertise in adverse event reporting, case processing, CAPA management, safety database operations, and regulatory compliance within the pharmaceutical and clinical research industry.
Author: Pharmabharat Editorial Team
Published on: May 21, 2026
Job Overview
| Details | Information |
|---|---|
| Company | QPS Bioserve India |
| Job Role | Junior Pharmacovigilance Associate / Drug Safety Associate |
| Experience | 3โ5 Years |
| Additional Role | Pharmacovigilance Associate / Drug Safety Associate |
| Senior Experience | 5โ10 Years |
| Location | Hyderabad |
| Industry | Pharmacovigilance / Drug Safety |
| Employment Type | Full-Time |
| Department | Clinical Safety & Pharmacovigilance |
QPS Bioserve Pharmacovigilance Job Responsibilities
Candidates selected for the Pharmacovigilance Associate role at QPS Bioserve will be responsible for handling end-to-end ICSR management and ensuring regulatory compliance.
Key Responsibilities
- Execute activities related to ICSR management within defined timelines
- Perform adverse event case follow-up with reporters, CROs, QC teams, and stakeholders
- Manage E2B XML submission of ICSRs to global regulatory authorities
- Handle safety database operational activities according to SOPs and pharmacovigilance regulations
- Support adverse event and product complaint handling processes
- Perform safety data reconciliation and data collection activities
- Contribute to CAPA development and process improvement initiatives
- Conduct pharmacovigilance training and support audit readiness
- Assist in health authority inspections and internal process audits
- Support medical coding conventions and systematic ICSR review improvements
- Coordinate cross-functional pharmacovigilance process enhancement initiatives
- Provide client notifications related to case management activities
Required Qualifications for Pharmacovigilance Associate Jobs
Educational Qualification
Candidates from the following backgrounds are preferred:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology or related healthcare disciplines
Experience Required
- 3โ5 years experience for Junior Pharmacovigilance Associate role
- 5โ10 years experience for Senior Pharmacovigilance Associate role
- Strong expertise in ICSR processing and regulatory reporting
- Experience with E2B XML submissions and safety databases
Essential Skills
- Pharmacovigilance operations
- Drug safety case processing
- ICSR lifecycle management
- Regulatory reporting
- Adverse event handling
- CAPA management
- Medical coding support
- Excellent communication and organizational skills
- Ability to multitask and work collaboratively
Why Join QPS Bioserve?
Working with QPS Bioserve offers professionals exposure to global pharmacovigilance operations, regulatory reporting systems, and advanced drug safety workflows.
Employee Benefits
- Opportunity to work on global PV projects
- Exposure to regulatory authority submissions
- Career growth in pharmacovigilance and clinical safety
- Collaborative work environment
- Training and audit exposure
- Experience with international safety standards and SOPs
How to Apply
Application Link For Junior Pharmacovigilance Associate / Drug Safety Associate
Application Link For Pharmacovigilance Associate / Drug Safety Associate
mail: hr@qpsbioserve.com