Job Overview
| Particulars | Details |
|---|---|
| Position | Multiple Healthcare & Life Sciences Openings |
| Company | Wipro |
| Job Type | |
| Experience | Fresher |
| Category / Department | Medical |
| Application Mode |
🏢 About Wipro
Wipro is a leading global technology services and consulting company delivering innovative digital transformation, engineering, healthcare, life sciences, and business process solutions. With operations across multiple countries, Wipro empowers organizations through technology, innovation, and highly skilled professionals while fostering continuous learning and career growth.
💡 Editor's Note / Preparation Tip
• Highlight Pharmacovigilance or Medical Device experience.
• Mention CAPA, FMEA, ISO 14971, and Risk Management expertise.
• Showcase analytical tools such as Excel, VBA, and Power BI.
• Include measurable achievements and certifications.
• Keep your resume ATS-friendly.
Interview Preparation
• Revise Drug Safety and Medical Device regulations.
• Review complaint investigation workflows.
• Practice scenario-based risk management questions.
• Refresh knowledge of CAPA and FMEA concepts.
• Prepare examples demonstrating communication and analytical skills.
Professional Tips
• Stay updated with global healthcare regulations.
• Develop strong documentation and reporting practices.
• Strengthen analytical and presentation skills.
• Learn Power BI and advanced Excel reporting.
• Demonstrate adaptability and teamwork during interviews.
📝 Job Description
🚀 Multiple Healthcare & Life Sciences Openings | Wipro
Looking to advance your career in Pharmacovigilance, Medical Devices, Drug Safety, Risk Management, Training, or MIS? Wipro is hiring experienced professionals across Pune, Kolkata, Gurgaon, and Hyderabad through Email Applications and Walk-In Interview Drives. If you have relevant healthcare, life sciences, medical device, or reporting experience, this is an excellent opportunity to join one of the world’s leading technology and business services companies.
Position Details
🏢 Company: Wipro
💼 Positions:
- Drug Safety Physician
- Deputy Manager (Trainer) – Medical Device Investigation
- Assistant Manager (MIS)
- Medical Device Complaint Investigation Specialist
📍 Locations:
- Pune
- Kolkata
- Hyderabad
- Gurgaon (Walk-In)
🏢 Work Mode: Work From Office
💼 Experience: 1–9 Years
🎓 Qualification:
- MBBS / MD (MCI Registered)
- B.Pharm
- Biomedical Engineering
- Nursing
- Life Science Graduates
- Life Science Postgraduates
- Any Graduate (For MIS)
📄 Employment Type: Full-Time
📅 Joining Preference: Immediate Joiners Preferred
Preferred Skills
✔ Medical Review Experience
✔ Trainer Experience
✔ Dashboard & MIS Reporting
✔ Regulatory Compliance
✔ Complaint Handling
✔ Night Shift Flexibility
✔ Immediate Availability
Candidate Requirements
• Relevant educational qualification as per the role.
• 1–9 years of relevant experience depending on the position.
• Strong communication and analytical skills.
• Knowledge of Drug Safety, Medical Devices, Risk Management, or MIS.
• Immediate joiners will be preferred.
• Willingness to work rotational/night shifts where applicable.
Why Join Wipro?
• Join a globally recognized healthcare and technology organization.
• Work on international Pharmacovigilance and Medical Device projects.
• Excellent career growth opportunities.
• Exposure to global healthcare clients.
• Collaborative and learning-focused work environment.
• Opportunities in Drug Safety, Risk Management, and Data Analytics.
• Continuous professional development.
• Competitive compensation and career progression.
Walk-In Interview Details
📍 Pune
Dates: 14–16 July 2026
Reporting Time: 10:00 AM – 12:00 PM
Venue:
Unit 2, Plot No. 31,
Hinjewadi Phase 2,
Rajiv Gandhi Info Tech Park,
Pune – 411057
Contact Persons: Varsha / Riya / Priyanka
📍 Gurgaon
Dates: 16–17 July 2026
Reporting Time: 10:00 AM – 12:00 PM
Venue:
Wipro HR Services India Pvt. Ltd.
Building 2,
Candor Techspace,
Sector 48,
Gurgaon, Haryana – 122001
Contact Person: Simran
📍 Hyderabad
Dates: 14–16 July 2026
Reporting Time: 10:00 AM – 12:00 PM
Venue:
Wipro Limited,
STPI Tower 6,
Manikonda,
Gachibowli,
Hyderabad – 500032
Contact Person: Pavan
Email Application
📧 Drug Safety Physician
Send your resume to:
📧 Deputy Manager (Trainer) – Medical Device Investigation
Send your resume to:
📧 Assistant Manager (MIS)
Send your resume to:
Documents to Carry
• Updated Resume/CV
• Original Government Photo ID
• Mention the source of the walk-in on the top of your CV
How to Apply
📧 Email Applications: Send your updated resume to:
🚶 Walk-In Candidates: Attend the interview on the scheduled dates with all required documents.
Know someone who would be a great fit? Tag them or share this opportunity with your network!
🎯 Key Responsibilities
- ✓ Perform medical review of drug safety cases and adverse event assessments.
- ✓ Investigate medical device complaints and support vigilance reporting.
- ✓ Execute risk assessments using CAPA, FMEA, and ISO 14971 methodologies.
- ✓ Deliver technical and process training for Medical Device Investigation teams.
- ✓ Prepare operational dashboards and MIS reports using Excel, VBA, and Power BI.
- ✓ Analyze operational trends and business performance metrics.
- ✓ Maintain compliance with global regulatory and quality standards.
- ✓ Collaborate with cross-functional and global healthcare teams.
- ✓ Support continuous process improvement initiatives.
💡 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 Multiple Healthcare & Life Sciences Openings 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
Q1. Which roles are currently open?
Drug Safety Physician, Deputy Manager (Trainer), Assistant Manager (MIS), and Medical Device Complaint Investigation Specialist.
Q2. Who can apply?
Eligible candidates with MBBS/MD, B.Pharm, Biomedical Engineering, Nursing, Life Science, or relevant graduate qualifications as specified for each role.
Q3. Is prior experience required?
Yes. Experience requirements range from 1–9 years depending on the position.
Q4. Are immediate joiners preferred?
Yes. Immediate joiners will be given preference.
Q5. What documents should candidates bring for the walk-in?
Updated Resume, Original Government Photo ID, and supporting documents.
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