Venus Remedies Pharmacovigilance Analyst Job 2026
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(Venus Remedies Pharmacovigilance Analyst Job 2026) |
Introduction
Venus Remedies Limited has announced a new hiring opportunity for experienced Pharmacovigilance professionals at its Panchkula office. The company is recruiting skilled candidates for the role of Pharmacovigilance Analyst to support global drug safety operations, EU regulatory compliance, signal detection, and aggregate safety reporting activities.
This latest Pharmacovigilance job in India is an excellent opportunity for B.Pharm, M.Pharm, Pharm.D, and Life Sciences graduates who want to build a long-term career in global Pharmacovigilance, post-marketing surveillance, and international regulatory affairs. Candidates with expertise in EudraVigilance, Argus Safety, MedDRA coding, and EU GVP modules will have a strong advantage during the selection process.
The role offers exposure to global safety databases, risk management activities, regulatory inspections, and international Pharmacovigilance processes within a reputed pharmaceutical organization.
About Venus Remedies Limited
Venus Remedies Limited is one of India’s leading research-driven pharmaceutical companies specializing in critical care medicines, oncology, anti-infectives, and high-end healthcare formulations. The company operates in multiple international markets and is recognized for its focus on innovation, regulatory compliance, and global healthcare solutions.
Founded in 1989, Venus Remedies is headquartered in Panchkula, Haryana, India. The organization has expanded its presence across more than 70 countries worldwide and continues strengthening its position in regulated pharmaceutical markets.
The company employs thousands of professionals globally and operates advanced manufacturing and research facilities approved by international regulatory authorities. Venus Remedies is widely known for maintaining high standards in Pharmacovigilance, quality systems, regulatory affairs, and drug safety operations.
Job Overview Summary
The Pharmacovigilance Analyst role at Venus Remedies focuses on handling global safety reporting activities, Individual Case Safety Reports (ICSRs), signal detection, and compliance with EU Pharmacovigilance regulations. Selected candidates will work closely with Regulatory Affairs, Medical Affairs, Quality Assurance, and Global Safety teams to maintain patient safety and ensure timely safety reporting.
This role is ideal for professionals seeking hands-on exposure to EU GVP modules, EudraVigilance reporting systems, aggregate safety reporting, and risk management plans within a global pharmaceutical environment.
Vacancy Details
| Particulars | Details |
|---|
| Job Title | Pharmacovigilance Analyst |
| Company | Venus Remedies Limited |
| Location | Panchkula |
| Industry | Pharmacovigilance / Drug Safety |
| Employment Type | Full-Time |
| Experience Required | 3 – 7 Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, Life Sciences |
| Application Mode | Online |
Job Role Explanation
The selected Pharmacovigilance Analyst will support multiple global drug safety activities related to post-marketing surveillance and regulatory compliance. The role requires professionals to review safety data, monitor adverse event reports, manage signal detection activities, and support aggregate safety reporting processes.
Candidates will also contribute to maintaining regulatory compliance with EMA guidelines, ICH standards, and EU GVP modules while ensuring the timely submission of safety data through global Pharmacovigilance systems.
This position offers excellent exposure to international drug safety workflows and regulatory reporting standards.
Key Responsibilities
Pharmacovigilance Operations
Selected candidates will be responsible for:
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Managing and reviewing Individual Case Safety Reports (ICSRs)
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Performing case triage and medical review activities
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Conducting MedDRA and WHO-DD coding
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Preparing safety narratives and case assessments
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Supporting causality assessment and benefit-risk evaluation
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Monitoring EudraVigilance reporting timelines
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Managing aggregate safety reports, such as:
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PSUR/PBRER
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DSUR
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Risk Management Plans (RMPs)
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Signal Evaluation Reports
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Supporting signal detection and validation activities
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Maintaining Pharmacovigilance SOPs and compliance documentation
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Participating in audits, inspections, and CAPA activities
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Collaborating with QA, Regulatory Affairs, and Medical Affairs teams
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Ensuring compliance with EU GVP Modules and ICH guidelines
Eligibility Criteria
Educational Qualification
Candidates must possess any of the following qualifications:
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B.Pharm
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M.Pharm
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Pharm.D
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Life Sciences Graduate
Experience Required
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Minimum 3 to 7 years of Pharmacovigilance experience
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Experience in global drug safety operations preferred
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Exposure to EU market Pharmacovigilance activities will be advantageous
Skills Required
Venus Remedies is looking for professionals with strong expertise in:
Technical Skills
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EU GVP Modules
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EudraVigilance Reporting
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EMA Pharmacovigilance Guidelines
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ICH Guidelines
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Signal Detection and Risk Management
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Aggregate Safety Reporting
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E2B(R3) Submissions
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MedDRA Coding
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WHO-DD Coding
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Regulatory Inspection Readiness
Safety Database Experience
Preferred candidates should have hands-on experience with:
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Argus Safety
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ArisG
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Oracle Safety Database
Soft Skills
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Analytical thinking
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Attention to detail
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Communication skills
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Team collaboration
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Documentation management
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Regulatory compliance understanding
Salary Estimate
Based on current Pharmacovigilance industry trends in India, the estimated salary for the Pharmacovigilance Analyst role at Venus Remedies may range between:
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₹7 LPA – ₹14 LPA (Approximate)
The final salary package may vary depending on:
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Pharmacovigilance experience
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EU market exposure
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Aggregate reporting expertise
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Safety database proficiency
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Regulatory compliance knowledge
Interview Details
Selection Process
The recruitment process may include:
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Resume Shortlisting
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HR Discussion
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Technical Pharmacovigilance Interview
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Final Managerial Round
Topics Commonly Covered in Interview
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ICSR processing
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EU GVP Modules
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Signal detection
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MedDRA coding
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EudraVigilance submissions
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Aggregate safety reporting
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Argus Safety workflows
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Case narrative writing
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Pharmacovigilance compliance
Required Documents
Candidates should keep the following documents ready while applying:
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Updated Resume/CV
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Educational Certificates
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Experience Certificates
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Latest Salary Slip
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Government ID Proof
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Passport Size Photograph
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Pharmacovigilance Training Certificates (if available)
Why Join Venus Remedies?
Working with Venus Remedies provides excellent exposure to global Pharmacovigilance operations and international drug safety standards.
Employee Benefits
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Exposure to EU regulatory reporting systems
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Hands-on Pharmacovigilance experience
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Career growth in global drug safety
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Opportunity to work on signal management projects
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Cross-functional collaboration with global teams
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Experience with advanced safety databases
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Stable long-term pharmaceutical career opportunities
Job Location
Work Location
Panchkula, Haryana, India
This is a full-time office-based Pharmacovigilance role.
How to Apply
Interested and eligible candidates can apply online through the official application link below:
Application Link:
Candidates are advised to carefully review the eligibility criteria and update their resumes before applying.
Frequently Asked Questions (FAQs)
Q1. What is the job role offered by Venus Remedies?
Venus Remedies is hiring candidates for the role of Pharmacovigilance Analyst.
Q2. What qualifications are required for this PV job?
Candidates with B.Pharm, M.Pharm, Pharm.D, and Life Sciences degrees can apply.
Q3. What experience is required for this role?
Applicants should have 3–7 years of Pharmacovigilance or drug safety experience.
Q4. Is experience with Argus Safety mandatory?
Hands-on experience with Argus Safety or similar safety databases is highly preferred.
Q5. What is the work location for this Pharmacovigilance role?
The job location is Panchkula, Haryana.
Q6. Is this role suitable for freshers?
No, this position is intended for experienced Pharmacovigilance professionals.
Q7. What are the important skills required?
EU GVP knowledge, EudraVigilance reporting, signal detection, aggregate reporting, and ICSR processing are important skills.
Q8. What is the estimated salary for this position?
The estimated salary range is approximately ₹7 LPA – ₹14 LPA, depending on experience and expertise.
Final Conclusion
The Venus Remedies Pharmacovigilance Analyst recruitment 2026 presents a valuable opportunity for experienced drug safety professionals seeking career growth in global Pharmacovigilance operations. Candidates with strong expertise in EU regulations, aggregate safety reporting, signal detection, and safety databases can gain excellent exposure to international drug safety practices within a reputed pharmaceutical company.
Professionals looking to advance their careers in Pharmacovigilance, regulatory compliance, and global safety reporting should consider applying for this opportunity at the earliest opportunity.
Disclaimer
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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