Wipro Hiring Drug Safety & Medical Device Specialists
Are you seeking Wipro Careers India or a Walk-in Interview for Drug Safety Jobs? Global technology and business service firm Wipro has announced multiple hiring opportunities across Pune, Kolkata, Hyderabad, and Gurgaon.
These clinical complaint investigations, medical reviews, risk evaluations, and MIS database report profiles operate full-time in a work-from-office capacity. The roles are open to candidates holding B.Pharm, MBBS, MD, Biomedical Engineering, Nursing, or related life science degrees. Wipro is hiring for Drug Safety Physicians, Medical Device Complaint Investigators, Trainers, and MIS Assistant Managers. Eligible specialists will track safety agreements, process adverse event timelines, perform CAPA investigations, and maintain operational statistics dashboards. To write a resume detailing your drug safety compliance, FMEA risk checklists, or database queries, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Hiring Positions Details
| Position | Location | Experience | Qualifications | Estimated CTC |
|---|---|---|---|---|
| Drug Safety Physician (Email Apply) | Pune (Work from Office) | 5 – 7 Years | MBBS / MD (MCI Registered) | ₹18 – ₹28 LPA |
| Deputy Manager - Trainer (Email Apply) | Pune / Kolkata | 6 – 9 Years | Any Life Science Graduate | ₹10 – ₹16 LPA |
| Assistant Manager - MIS (Email Apply) | Pune / Kolkata | 6 – 9 Years | Any Graduate (Excel, VBA, Power BI) | ₹8 – ₹14 LPA |
| Medical Device Complaint Investigation (Walk-In) | Pune, Gurgaon, Hyderabad | 1 – 5 Years | B.Pharm, Bio-med, Nursing, BSc / MSc Life Sciences | ₹5 – ₹9 LPA |
💼 Key Responsibilities by Position
1. Drug Safety Physician
- Perform medical review of clinical drug safety cases and validate adverse events.
- Assess causality, write clinical safety summaries, and ensure global regulatory compliance.
- Collaborate with international safety boards regarding aggregate documentation checks.
2. Deputy Manager (Trainer) – Medical Device Investigation
- Deliver technical training modules for Medical Device Complaint Investigation units.
- Handle complaint investigations, root cause analyses, FMEA audits, and CAPA.
- Ensure compliance guidelines meet ISO 14971 standards.
3. Assistant Manager (MIS)
- Prepare operational dashboards, track productivity statistics, and compile performance summaries.
- Develop automated tracking tools using Advanced Excel, VBA macros, and Power BI dashboards.
4. Medical Device Complaint Investigation (Walk-In Roles)
- Investigate medical device complaints and safety failures reported by healthcare institutions.
- Perform safety risk evaluations, compile CAPA timelines, and support vigilance report submissions.
To learn how pharmacovigilance safety physician salaries compare to conventional data coding and statistics careers, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Physicians: Valid MBBS or MD degree with mandatory MCI registration.
- Medical Devices: Experience in CAPA, FMEA, complaint handling, and ISO 14971 validation.
- MIS Analysts: Strong proficiency in VBA coding, dashboard creation, and performance reporting.
- Communication: Strong English communication skills and comfortable with rotational/night shifts.
For pharmacy and engineering graduates evaluating medical device vigilance careers compared to conventional laboratory quality control or formulation desks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Wipro Healthcare?
- Work for a global leader in clinical processing and healthcare lifecycle services.
- Obtain exposure to advanced medical device portfolios and global safety projects.
- Clear career progression routes into operations management and technical leadership.
- Competitive salaries, shift allowance, and comprehensive insurance benefits.
To review your basic knowledge of patient registries, medical devices, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Complaint Investigation vs Healthcare IT
Wipro Medical Device Complaint Investigation specialists track safety logs, audit risk files, and perform CAPA reports, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Wipro Walk-In Candidates
- Mention Risk Tools: List tools like FMEA, fishbone analysis, or 5-Why methodology you used in complaint handling.
- Detail MCI Registry: Safety physicians must clearly state their MCI registration number in the resume header.
- Highlight VBA Projects: MIS applicants should detail specific macro automations they designed.
💬 Wipro Healthcare Selection Interview Questions
- Q1. What is the difference between a correction, corrective action, and preventive action (CAPA)?
Answer Guidance: A correction is immediate action taken to eliminate a detected nonconformity. A corrective action prevents recurrence by targeting the root cause. A preventive action prevents occurrence by addressing a potential issue. - Q2. How is risk evaluated under ISO 14971 standards?
Answer Guidance: Risk is evaluated by assessing the probability of occurrence of harm combined with the severity of that harm, utilizing tools like FMEA (Failure Mode and Effects Analysis) to define risk levels. - Q3. What is medical review in pharmacovigilance?
Answer Guidance: Medical review is the evaluation of case data by a physician to ensure clinical plausibility, correct coding of terms (MedDRA), validation of causality assessments, and clinical narrative accuracy.
📖 How to Apply?
Before submitting your application, please read the step-by-step guidance on how to navigate the registration portal, fill out required forms, and format your application profile:
📄 Premium ATS Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Drug Safety, Medical Devices, or MIS reporting roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 Direct Application & Walk-in Details
Submit your application via email or attend the walk-in interviews at the dates and venues listed below:
📧 Email Application (For Safety Physicians, Trainers & MIS):
Send your updated resume to:
• ishita.jhanwar1@wipro.com
• and copy radha.hubli1@wipro.com
🚶 Walk-In Interview Venues (Medical Device Investigation roles only):
📍 Pune Drive: 14–16 July 2026 (10 AM – 12 PM)
Venue: Unit 2, Plot No. 31, Hinjewadi Phase 2, Rajiv Gandhi Info Tech Park, Pune – 411057 (Contact: Varsha / Riya / Priyanka)
📍 Gurgaon Drive: 16–17 July 2026 (10 AM – 12 PM)
Venue: Wipro HR Services India Pvt. Ltd., Building 2, Candor Techspace, Sector 48, Gurgaon, Haryana – 122001 (Contact: Simran)
📍 Hyderabad Drive: 14–16 July 2026 (10 AM – 12 PM)
Venue: Wipro Limited, STPI Tower 6, Manikonda, Gachibowli, Hyderabad – 500032 (Contact: Pavan)
*Carry your updated CV, Gov Photo ID, and write "Source: Walk-in" on top of your resume.
❓ Frequently Asked Questions
Q. Which qualifications are eligible for the Walk-in Drive?
B.Pharm, Biomedical Engineering, Nursing, BSc / MSc Life Sciences, or related postgraduates are eligible for the Medical Device Complaint Investigation walk-ins.
Q. What is the shift schedule for these roles?
Most roles require working in rotational or night shifts. Drug Safety Physicians will work rotational shifts.
Q. How should I apply for the Trainer or MIS role?
Please email your resume directly to ishita.jhanwar1@wipro.com and radha.hubli1@wipro.com as these roles are processed via email screening.
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