QPS Bioserve India Hiring Pharmacovigilance Associates in Hyderabad | Drug Safety Jobs 2026
QPS Bioserve India Hiring Pharmacovigilance Associates and Drug Safety Associates in Hyderabad
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(QPS Bioserve India Hiring Pharmacovigilance Associates in Hyderabad) |
Introduction
QPS Bioserve India has announced multiple openings for experienced Pharmacovigilance professionals in Hyderabad for the positions of Junior Pharmacovigilance Associate, Pharmacovigilance Associate, and Drug Safety Associate. These pharmaceutical and clinical safety jobs are ideal for candidates with strong expertise in ICSR management, regulatory reporting, E2B XML submissions, pharmacovigilance operations, and drug safety case processing.
Candidates with qualifications in Pharmacy, Life Sciences, Biotechnology, and related healthcare disciplines, along with relevant industry experience,e are encouraged to apply for these latest pharmacovigilance jobs in Hyderabad.
This opportunity provides excellent exposure to global pharmacovigilance operations, adverse event reporting systems, drug safety workflows, CAPA management, regulatory compliance, and international clinical safety standards.
Professionals looking to grow their careers in Pharmacovigilance, Clinical Safety, Drug Safety Operations, and Regulatory Reporting should not miss this opportunity.
About QPS Bioserve India
Company Overview
QPS Bioserve India is a leading global Contract Research Organization (CRO) and clinical research service provider specializing in pharmacovigilance, drug safety, bioanalysis, clinical trials, and regulatory support services.
The company operates as part of QPS Holdings, a globally recognized CRO organization serving pharmaceutical, biotechnology, and healthcare companies across multiple international markets.
QPS Bioserve India has established a strong reputation for delivering:
- Pharmacovigilance Services
- Drug Safety Operations
- Clinical Research Support
- Bioanalytical Services
- Regulatory Compliance Solutions
- Clinical Data Management
- Medical Writing Services
The organization focuses heavily on quality systems, regulatory compliance, global safety standards, and advanced pharmacovigilance technologies.
Headquarters and Global Presence
| Particulars | Details |
|---|---|
| Company Name | QPS Bioserve India |
| Parent Organization | QPS Holdings LLC |
| Industry | Clinical Research & Pharmacovigilance |
| Headquarters | Hyderabad, Telangana, India |
| Global Headquarters | Newark, Delaware, USA |
| Founded | 1995 |
| Employees | 1,000+ Globally |
| Specialization | Drug Safety, Clinical Research, Pharmacovigilance |
QPS Bioserve works with global pharmaceutical and biotechnology companies and supports multiple international clinical safety programs and regulatory reporting operations.
Job Overview Summary
QPS Bioserve India is currently hiring experienced candidates for multiple Pharmacovigilance and Drug Safety positions in Hyderabad.
The company is recruiting for:
- Junior Pharmacovigilance Associate / Drug Safety Associate
- Pharmacovigilance Associate / Drug Safety Associate
Selected candidates will handle end-to-end ICSR lifecycle management, adverse event reporting, E2B XML submissions, safety database operations, CAPA management, and pharmacovigilance compliance activities.
These roles offer excellent opportunities for professionals interested in:
- Pharmacovigilance Operations
- Drug Safety Case Processing
- Clinical Safety Management
- Regulatory Reporting
- ICSR Management
- Adverse Event Reporting
- Global PV Compliance
- Safety Database Operations
Candidates with prior exposure to international pharmacovigilance processes and global regulatory standards will have an advantage.
Vacancy Details
| Details | Information |
|---|---|
| Company | QPS Bioserve India |
| Department | Clinical Safety & Pharmacovigilance |
| Job Role | Junior Pharmacovigilance Associate / Drug Safety Associate |
| Additional Role | Pharmacovigilance Associate / Drug Safety Associate |
| Experience Required | 3–10 Years |
| Location | Hyderabad |
| Employment Type | Full-Time |
| Industry | Pharmacovigilance / Drug Safety |
Job Role Explanation
Pharmacovigilance Associate / Drug Safety Associate
The selected candidates will work in the Clinical Safety and Pharmacovigilance department and support global drug safety operations.
Primary responsibilities include:
- Managing ICSR workflows
- Performing adverse event follow-ups
- Regulatory reporting
- Safety database management
- CAPA implementation
- Pharmacovigilance compliance activities
- Safety data reconciliation
- Audit and inspection support
Candidates will collaborate with internal teams, CROs, quality control teams, healthcare professionals, and regulatory stakeholders.
This role is highly suitable for professionals looking to build long-term careers in:
- Pharmacovigilance
- Clinical Safety
- Drug Safety Operations
- Medical Coding
- Regulatory Affairs
- Clinical Research
- Global PV Compliance
Key Responsibilities
Selected candidates will handle multiple pharmacovigilance and drug safety responsibilities.
Major Responsibilities Include
- Executing ICSR management activities within defined timelines
- Performing adverse event case follow-ups with reporters and stakeholders
- Managing E2B XML submissions to global regulatory authorities
- Supporting safety database operational activities
- Handling adverse events and product complaint management processes
- Performing safety data reconciliation activities
- Supporting CAPA development and process improvement initiatives
- Conducting pharmacovigilance training activities
- Supporting health authority inspections and audits
- Assisting in medical coding conventions and systematic case reviews
- Coordinating pharmacovigilance process enhancement activities
- Providing client notifications related to drug safety case management
Candidates will also gain exposure to international pharmacovigilance standards and global regulatory systems.
Eligibility Criteria
Educational Qualification
Candidates from the following backgrounds are eligible to apply:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology
- Healthcare-related disciplines
Experience Required
Junior Pharmacovigilance Associate
- 3–5 years of relevant experience
Pharmacovigilance Associate / Drug Safety Associate
- 5–10 years of relevant experience
Candidates should possess strong expertise in:
- ICSR Processing
- Regulatory Reporting
- Safety Databases
- E2B XML Submissions
- Pharmacovigilance Operations
Job Location
- Hyderabad, Telangana, India
Skills Required
Candidates should possess both technical and behavioral skills.
Technical Skills
- Pharmacovigilance operations
- ICSR lifecycle management
- Drug safety case processing
- Regulatory reporting
- E2B XML submissions
- Adverse event handling
- CAPA management
- Medical coding support
- Safety database operations
- Audit and inspection readiness
Behavioral Skills
- Strong communication skills
- Organizational ability
- Attention to detail
- Multitasking capability
- Team collaboration
- Process improvement mindset
Candidates with global PV process exposure will have an added advantage.
Salary Estimate
Based on current pharmacovigilance industry standards in Hyderabad, the estimated salary range is:
Estimated Salary Range
Junior Pharmacovigilance Associate
₹5 LPA – ₹8 LPA
Pharmacovigilance Associate / Drug Safety Associate
₹8 LPA – ₹15 LPA
Actual compensation may vary depending on:
- Experience level
- Regulatory reporting expertise
- Safety database knowledge
- Interview performance
- Global PV exposure
Why Join QPS Bioserve India?
Working at QPS Bioserve offers professionals strong exposure to international pharmacovigilance operations and clinical safety systems.
Employee Benefits
- Exposure to global PV projects
- International regulatory submission experience
- Career growth in drug safety and pharmacovigilance
- Collaborative work environment
- Audit and inspection exposure
- Training opportunities
- SOP and compliance management experience
Employees gain valuable experience working with global pharmaceutical clients and advanced safety systems.
Interview Details
Company Name
QPS Bioserve India
Department
Clinical Safety & Pharmacovigilance
Positions Available
- Junior Pharmacovigilance Associate
- Pharmacovigilance Associate
- Drug Safety Associate
Location
Hyderabad
Experience Required
3–10 Years
Apply Mode
Online Application
How to Apply
Interested candidates can apply online through the official Naukri application links provided below.
Application Link – Junior Pharmacovigilance Associate / Drug Safety Associate
Application Link – Pharmacovigilance Associate / Drug Safety Associate
Candidates should apply with updated resumes highlighting their pharmacovigilance, ICSR processing, and regulatory reporting experience.
Required Documents
Candidates should keep the following documents ready before applying:
- Updated Resume/CV
- Educational Certificates
- Experience Certificates
- Latest Salary Slip
- Government ID Proof
- Passport Size Photograph
- Pharmacovigilance Training Certificates
- Regulatory Reporting Experience Details
- Safety Database Experience Information
Candidates are advised to maintain ATS-friendly resumes focused on pharmacovigilance and drug safety skills.
Frequently Asked Questions (FAQs)
1. Which company is hiring for these pharmacovigilance roles?
QPS Bioserve India is hiring experienced Pharmacovigilance and Drug Safety professionals in Hyderabad.
2. What positions are available?
The company is hiring for:
- Junior Pharmacovigilance Associate
- Pharmacovigilance Associate
- Drug Safety Associate
3. What qualifications are required?
Candidates with B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related healthcare backgrounds can apply.
4. What experience is required?
Candidates with 3–10 years of pharmacovigilance and drug safety experience are eligible.
5. What technical skills are preferred?
ICSR processing, E2B XML submissions, regulatory reporting, safety databases, adverse event handling, and CAPA management.
6. What is the expected salary range?
The estimated salary range is ₹5 LPA – ₹15 LPA, depending on role and experience.
7. What is the job location?
The job location is Hyderabad, Telangana.
8. What type of exposure will candidates receive?
Candidates will gain exposure to global pharmacovigilance operations, regulatory submissions, clinical safety workflows, and international compliance systems.
Final Conclusion
QPS Bioserve India has opened excellent career opportunities for experienced pharmacovigilance professionals seeking growth in Clinical Safety, Drug Safety Operations, and Regulatory Reporting. These Pharmacovigilance Associate and Drug Safety Associate roles in Hyderabad provide strong exposure to global ICSR management, adverse event reporting, E2B submissions, CAPA systems, and pharmacovigilance compliance operations.
Professionals with expertise in pharmacovigilance workflows, safety databases, and regulatory reporting can significantly strengthen their long-term pharmaceutical careers through this opportunity.
Working with QPS Bioserve India offers candidates valuable international exposure, career growth opportunities, and experience with global clinical safety operations.
Interested candidates should apply as early as possible through the official application links.
Disclaimer
This job information is provided for educational and informational purposes only. Candidates are advised to verify recruitment details from the official company website before applying. Pharma Duniya is not responsible for recruitment processes, interview schedules, or hiring decisions made by the company.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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