Candidates with relevant experience in ICSR processing, PSUR activities, adverse event handling, safety databases, and global pharmacovigilance workflows are encouraged to attend the drive.
Job Overview
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance Professional – SPE / SME |
| Company | Cognizant |
| Job Type | Full-Time |
| Category / Department | Research |
| Application Mode | Online |
💡 Editor's Note / Preparation Tip
📝 Editorial Notes
📌 This recruitment drive is specifically intended for experienced Pharmacovigilance professionals.
📌 Freshers should not attend this particular walk-in unless the eligibility criteria are officially changed.
📌 Candidates should carefully match their experience with the SPE or SME requirements.
📌 Professionals with ICSR Case Processing and PSUR exposure should highlight these skills prominently.
📌 Verify the venue, timings, eligibility, and recruitment details before travelling.
📌 Candidates should carry original documents as well as photocopies where appropriate.
📄 Resume Preparation Tips
1️⃣ Clearly mention your total Pharmacovigilance experience and relevant years of experience.
2️⃣ Highlight ICSR Case Processing, PSUR, Drug Safety, and Medical Review experience.
3️⃣ Mention the safety databases, case management systems, and relevant tools you have worked with.
4️⃣ Add measurable achievements related to quality, productivity, compliance, and turnaround time where possible.
5️⃣ Keep your resume concise, ATS-friendly, and focused on Pharmacovigilance responsibilities.
🎯 Interview Preparation
1️⃣ Revise the complete ICSR case processing lifecycle and key pharmacovigilance concepts.
2️⃣ Prepare to explain your experience with adverse event reports and safety case management.
3️⃣ Review PSUR concepts, regulatory reporting timelines, and relevant compliance requirements.
4️⃣ Be prepared to discuss quality checks, SOP adherence, deviations, and case-processing challenges.
5️⃣ Prepare real examples that demonstrate your attention to detail, decision-making, teamwork, and ability to meet deadlines.
💡 Professional Tips
🚀 Quantify your experience wherever possible, such as number of cases handled or quality metrics achieved.
🔬 Keep yourself updated on global Pharmacovigilance regulations and safety reporting practices.
📚 Understand the difference between case processing, medical review, aggregate reporting, and signal-related activities.
🤝 Demonstrate your ability to work effectively with global teams and cross-functional stakeholders.
📈 For SME-level roles, showcase mentoring, quality oversight, process improvement, and subject-matter expertise.
📝 Job Description
🚨 COGNIZANT WALK-IN DRIVE | PHARMACOVIGILANCE PROFESSIONALS 💊🔬
Looking to take the next step in your Pharmacovigilance or Drug Safety career? Cognizant is conducting a walk-in recruitment drive for experienced Pharmacovigilance professionals in Mumbai and Pune.
With 40 openings across different experience levels, this opportunity is suitable for professionals with hands-on exposure to ICSR Case Processing, PSUR, Medical Safety, and Drug Safety Operations.
⚠️ Important: This drive is for experienced candidates only. Freshers are not eligible.
📌 Job Details
🏢 Company: Cognizant
💼 Role: Pharmacovigilance Professional – SPE / SME
📋 Employment Type: Full-Time | Permanent
🎓 Qualification: B.Pharm / M.Pharm
💼 Experience: 1–8 Years
📍 Locations: Mumbai & Pune
👥 Total Openings: 40
💰 Salary: Competitive and based on relevant experience
📅 Walk-in Date: 1 August 2026
⏰ Walk-in Time: 10:00 AM – 1:00 PM
🔬 Open Positions
1️⃣ Senior Process Executive (SPE)
💼 Experience: 1–4 Years
🔹 Pharmacovigilance case processing
🔹 ICSR management
🔹 Safety database activities
🔹 Drug safety operations
2️⃣ Subject Matter Expert (SME)
💼 Experience: 4–8 Years
🔹 Advanced pharmacovigilance case processing
🔹 PSUR-related activities
🔹 Safety reporting and review
🔹 Pharmacovigilance operations
🎓 Eligibility Criteria
✔ B.Pharm or M.Pharm qualification
✔ 1–8 years of relevant Pharmacovigilance experience
✔ Experience with ICSR Case Processing
✔ Knowledge of PSUR processes
✔ Understanding of Drug Safety Operations
✔ Familiarity with pharmacovigilance workflows
✔ Knowledge of safety reporting processes
✔ Understanding of regulatory compliance requirements
❌ Freshers are not eligible for this walk-in drive
📍 Walk-In Venue – PUNE
📅 Date: 1 August 2026
⏰ Time: 10:00 AM – 1:00 PM
📍 Venue:
Phase 3, Plot No. 26
MIDC, Rajiv Gandhi Infotech Park
Hinjewadi, Pune – 411057
🏠 Location Eligibility: Candidates are expected to reside within approximately 20–30 KM of the Cognizant office.
📍 Walk-In Venue – MUMBAI
📅 Date: 1 August 2026
⏰ Time: 10:00 AM – 1:00 PM
📍 Venue:
2nd Floor, Building No. 9
Mindspace
Airoli East, Navi Mumbai
📌 Landmark: Opposite Airoli Railway Station
🎫 Entry Process: A QR code is available at Gate No. 1 for Mindspace entry.
🏠 Eligible Residential Areas – MUMBAI REGION
✔ Kalyan to CST
✔ Bhayander to Churchgate
✔ CBD Belapur to CST
✔ Thane to CBD Belapur
🌟 Why Consider Joining Cognizant?
🌍 Exposure to global healthcare and pharmaceutical projects
💊 Opportunity to work in Pharmacovigilance and Drug Safety operations
🚀 Potential career growth in a multinational organization
📚 Learning and professional development opportunities
🤝 Collaboration with global teams and industry professionals
🏢 Stable corporate work environment
💰 Competitive compensation based on experience
🌱 Employee wellness and professional development initiatives
🔬 Exposure to international Pharmacovigilance processes
📂 Documents To Carry
Candidates attending the walk-in interview should carry:
✔ Updated Resume / CV
✔ Passport-size photographs
✔ Government-issued ID proof
✔ Educational certificates
✔ Previous employment / experience certificates
✔ Latest salary slips
✔ PAN Card
✔ Aadhaar Card
⚠️ Important Walk-In Notes
📌 Attend the interview at your preferred location on 1 August 2026.
📌 Interview window: 10:00 AM to 1:00 PM.
📌 Candidates arriving after 1:00 PM may not be permitted to participate.
📌 Freshers are not eligible for this recruitment drive.
📌 Carry all required documents to avoid delays during the selection process.
📌 Candidates should verify the walk-in details with the official recruitment source before travelling.
📩 How to Apply
Interested and eligible candidates should directly attend the walk-in interview at their preferred location on 1 August 2026 between 10:00 AM and 1:00 PM.
📍 Pune:
Phase 3, Plot No. 26, MIDC, Rajiv Gandhi Infotech Park, Hinjewadi, Pune – 411057
📍 Mumbai:
2nd Floor, Building No. 9, Mindspace, Airoli East, Navi Mumbai
Landmark: Opposite Airoli Railway Station
📌 Bring all required documents and an updated resume.
🎯 Key Responsibilities
- ✓ Process Individual Case Safety Reports (ICSRs) according to established procedures.
- ✓ Support end-to-end pharmacovigilance case management activities.
- ✓ Review and process adverse event and safety information.
- ✓ Contribute to PSUR preparation and review activities, where applicable.
- ✓ Maintain accurate medical safety documentation and case records.
- ✓ Follow applicable pharmacovigilance regulations, SOPs, and quality standards.
- ✓ Meet defined quality standards and regulatory timelines.
- ✓ Support safety database-related activities.
- ✓ Collaborate with global pharmacovigilance and drug safety teams.
- ✓ Contribute to ongoing drug safety and operational activities.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Pharmacovigilance Professional – SPE / SME role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1️⃣ Who can attend this walk-in drive?
Candidates with a B.Pharm or M.Pharm qualification and 1–8 years of relevant Pharmacovigilance experience are eligible based on the stated requirements.
2️⃣ Are freshers eligible?
No. This particular walk-in drive is intended for experienced Pharmacovigilance professionals.
3️⃣ What roles are available?
The drive includes opportunities aligned with Senior Process Executive (SPE) and Subject Matter Expert (SME) profiles.
4️⃣ Where can candidates attend the interview?
Candidates can attend at either the Pune or Mumbai/Navi Mumbai venue, subject to the applicable location eligibility requirements.
5️⃣ What should candidates bring?
Carry an updated resume, passport-size photographs, government ID, educational and experience certificates, latest salary slips, PAN Card, and Aadhaar Card.
6️⃣ What time should candidates arrive?
The walk-in window is 10:00 AM to 1:00 PM on 1 August 2026. Candidates arriving after 1:00 PM may not be permitted.
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