Cognizant has announced an opening for the position of SPE-Pharmacovigilance in Mumbai, Maharashtra. This is a hybrid opportunity for professionals with hands-on experience in Pharmacovigilance, PV data management, case processing, drug safety, and pharmaceutical research and development.
The role involves monitoring drug safety information, processing adverse event data, supporting regulatory submissions, conducting quality reviews, and collaborating with global pharmacovigilance teams.
Cognizant Pharmacovigilance Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | Cognizant |
| Job Role | SPE-Pharmacovigilance |
| Job ID | 00067689992 |
| Job Location | Mumbai, Maharashtra |
| Work Mode | Hybrid |
| Employment Type | Full-Time |
| Work Shift | Day Shift |
| Travel | No Travel Required |
| Functional Area | Pharmacovigilance / Pharma R&D |
| Published Date | August 13, 2026 |
| Application Mode | Online |
Job Summary
The SPE-Pharmacovigilance professional will support drug safety monitoring, PV case processing, pharmacovigilance data management, safety reporting, and regulatory compliance activities.
The selected candidate will work with cross-functional and global teams to ensure accurate handling of safety data and timely reporting of adverse events. The role also includes supporting process improvements, quality audits, training, risk management activities, and regulatory documentation.
Key Responsibilities
The selected candidate will be responsible for:
- Monitoring and evaluating drug safety data.
- Ensuring pharmacovigilance activities comply with regulatory requirements and company policies.
- Processing and managing pharmacovigilance case data.
- Collaborating with cross-functional teams to analyze safety information.
- Interpreting pharmacovigilance data for accurate reporting.
- Developing strategies to improve PV case processing and data management efficiency.
- Providing insights based on safety data analysis.
- Ensuring accurate and timely documentation of adverse event reports.
- Supporting safety assessments and regulatory reporting activities.
- Assisting with regulatory submissions and safety reports.
- Conducting audits of pharmacovigilance processes.
- Identifying quality and process improvement opportunities.
- Supporting quality control activities within PV operations.
- Conducting training sessions for team members on pharmacovigilance processes.
- Using pharmacovigilance software and tools for data collection and analysis.
- Coordinating with global teams to maintain consistency in PV operations.
- Supporting risk management plans and safety monitoring strategies.
- Keeping updated with changes in pharmacovigilance regulations and industry practices.
Educational and Professional Background
The job description emphasizes a strong background in Pharma Research & Development along with hands-on pharmacovigilance experience.
Candidates should have practical knowledge of:
- Pharmacovigilance
- Drug Safety
- PV Data Management
- ICSR Case Processing
- Adverse Event Reporting
- Safety Data Analysis
- Regulatory Compliance
- Pharmacovigilance Systems
- Safety Reporting
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Required Skills
Candidates should demonstrate:
- Strong pharmacovigilance knowledge.
- Hands-on experience in PV case processing and data management.
- Excellent attention to detail.
- Strong analytical and problem-solving abilities.
- Ability to interpret complex safety data.
- Proactive approach to identifying and resolving drug safety issues.
- Knowledge of pharmacovigilance software and tools.
- Strong written and verbal communication skills.
- Ability to collaborate with cross-functional and global teams.
- Willingness to continuously learn about new regulations and PV practices.
Certifications Required
The provided job description lists the following certifications:
- Certified Pharmacovigilance Professional (CPP)
- Advanced Pharmacovigilance Certification
Candidates should review the official job posting carefully to confirm certification requirements before applying.
Work Location and Schedule
Location: Mumbai, Maharashtra, India
Work Model: Hybrid
Shift: Day Shift
Travel: No travel required
The hybrid model provides a combination of office-based and remote working, subject to Cognizant’s applicable policies and role requirements.
Salary Details
Cognizant has not provided a specific salary range for the SPE-Pharmacovigilance position in the supplied job description.
The final compensation may depend on the candidate’s qualifications, pharmacovigilance experience, technical expertise, certifications, and interview performance.
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Career Opportunity
This role can be a valuable opportunity for professionals looking to develop their careers in Pharmacovigilance and Drug Safety.
The position provides exposure to:
- PV Case Processing
- Drug Safety Data Management
- Adverse Event Reporting
- Regulatory Submissions
- Safety Assessments
- Risk Management Plans
- PV Quality Audits
- Global Pharmacovigilance Operations
- Safety Monitoring Strategies
- Pharmacovigilance Technology
This experience can support future career growth in Drug Safety, Pharmacovigilance Operations, PV Quality, Safety Data Management, and Regulatory Safety.
How to Apply
Interested and eligible candidates can apply online through the Cognizant careers portal for the SPE-Pharmacovigilance position.
Job ID: 00067689992
Candidates should ensure their resume highlights relevant experience in PV case processing, pharmacovigilance data management, adverse event reporting, drug safety, regulatory compliance, and PV systems.
Frequently Asked Questions (FAQs)
What is the job role at Cognizant?
Cognizant is hiring for SPE-Pharmacovigilance.
Where is the job located?
The position is based in Mumbai, Maharashtra.
Is this a remote job?
The position follows a hybrid work model.
Is travel required?
The job description states that no travel is required.
What type of experience is required?
Candidates should have hands-on experience in Pharmacovigilance, PV data management, and case processing, along with a strong Pharma R&D background.
What certifications are mentioned?
The job posting lists Certified Pharmacovigilance Professional (CPP) and Advanced Pharmacovigilance Certification.
What are the main responsibilities?
The major responsibilities include drug safety monitoring, PV case processing, safety data management, regulatory reporting, quality audits, process improvement, training, and global PV coordination.
