SME – Pharmacovigilance
Company: Cognizant
Job Title: Subject Matter Expert (SME) – Pharmacovigilance
Job ID: 00068127491
Date Posted: July 10, 2026
Location: Mumbai, Maharashtra, India
Work Model: Hybrid
Job Category: Technology & Engineering
Experience Required
2–4 years of relevant experience in Pharmacovigilance.
Educational Qualification
The job posting does not explicitly mention educational qualifications. Typically, candidates with the following backgrounds are preferred:
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
B.Sc. / M.Sc. (Life Sciences)
Pharm.D
Other Life Sciences degrees with relevant Pharmacovigilance experience
Job Summary
Cognizant is looking for a Subject Matter Expert (SME) in Pharmacovigilance with 2–4 years of experience. The role focuses on pharmacovigilance data management, PV case processing, regulatory compliance, and drug safety. The selected candidate will collaborate with cross-functional teams to ensure the safety and effectiveness of pharmaceutical products while supporting global regulatory requirements.
Key Responsibilities
Analyze pharmacovigilance data to ensure regulatory compliance.
Support the development and implementation of pharmacovigilance strategies.
Provide expert guidance on PV case processing.
Ensure timely and accurate reporting of adverse events.
Monitor pharmacovigilance systems and recommend process improvements.
Maintain comprehensive documentation of PV activities.
Prepare regulatory submissions and safety reports.
Stay updated with the latest pharmacovigilance regulations and industry trends.
Train and mentor team members on PV processes.
Ensure data integrity and quality across pharmacovigilance activities.
Participate in audits and regulatory inspections.
Promote a culture of patient safety and regulatory compliance.
Required Skills
Pharmacovigilance
PV Data Management
ICSR Case Processing
Adverse Event Reporting
Pharma Research & Development
Regulatory Compliance
Safety Data Analysis
Documentation Management
Analytical and Problem-Solving Skills
Communication and Team Collaboration
Preferred Qualifications
Strong understanding of global pharmacovigilance regulations.
Experience in pharmaceutical research and development.
Ability to analyze complex safety data.
Knowledge of pharmacovigilance databases and workflows.
Experience supporting regulatory submissions and inspections.
Preferred Certification
Certified Pharmacovigilance Professional (CPP) or an equivalent certification (Preferred but not mandatory).
Work Model
Hybrid (Combination of office and remote work)
Estimated Salary Package
The official job posting does not disclose the salary. Based on industry standards for Mumbai:
|
Experience |
Estimated Annual CTC |
|---|---|
|
2–3 years |
₹5.5 – ₹8.5 LPA |
|
3–4 years |
₹7.0 – ₹10.5 LPA |
Expected Average CTC: ₹6–9 LPA, depending on experience, technical expertise, interview performance, and internal compensation policies.
Who Should Apply
Candidates with:
2–4 years of Pharmacovigilance experience.
Experience in PV case processing and safety data management.
Strong understanding of global regulatory requirements.
Good analytical, communication, and documentation skills.
Ability to work in a collaborative hybrid environment.
Location
Mumbai, Maharashtra, India
Employment Type
Full-time
Hybrid Work Model
Key Highlights
Opportunity to work as a Pharmacovigilance Subject Matter Expert.
Hybrid work environment.
Exposure to global pharmacovigilance regulations and drug safety projects.
Involvement in regulatory submissions, audits, and process improvements.
Career growth within one of the world's leading technology and healthcare services companies.
Collaborative work culture with opportunities for continuous learning and professional development.
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