Wipro hiring Freshers | Medical Device Investigator
- Wipro Walk‑In Drive 2026 | Medical Device Investigator | Freshers & Experienced | Kolkata, Hyderabad, Pune
- Company Overview
- Job Role & Responsibilities – Medical Device Investigator
- Key Responsibilities
- Eligibility & Qualifications
- Educational Qualifications (Freshers & Experienced)
- Experience Criteria
- Required Skills
- Walk‑In Details – Kolkata (Freshers)
- Walk‑In Details – Hyderabad (Interview Location) | Job Location Pune
- Walk‑In Details – Pune (Experienced Candidates)
- Why This Role Matters in Medical Device Compliance
- Career Growth Opportunities
- Frequently Asked Questions (FAQs)
- 1. Are freshers eligible?
- 2. Is experience mandatory for Hyderabad and Pune drives?
- 3. What documents should be carried?
- 4. Is rotational shift mandatory?
- 5. Can candidates with other qualifications attend?
- Summary Table
Wipro Walk‑In Drive 2026 | Medical Device Investigator | Freshers & Experienced | Kolkata, Hyderabad, Pune
entity[“organization”,”Wipro”,”information technology company”] is conducting multiple walk‑in drives for the role of Medical Device Investigator across Kolkata, Hyderabad, and Pune. These opportunities are open for both freshers and experienced professionals in life sciences, pharmacy, medical technology, and allied healthcare disciplines.
For freshers, the walk‑in drive will be held in Kolkata on 23rd, 24th, and 25th February 2026. For experienced candidates with 3–5 years of medical device investigation experience, walk‑ins are scheduled in Hyderabad (interview location for Pune job role) on 25th & 26th February and in Pune on 23rd & 24th February 2026.
If you are looking to build or advance your career in medical device investigation, complaint handling, regulatory compliance, and EU MDR-aligned safety evaluation, this is a strong opportunity with a globally recognized organization.
Company Overview
Wipro is a global technology and consulting leader delivering digital transformation, regulatory solutions, and healthcare compliance services across industries. With operations in multiple countries, Wipro supports pharmaceutical, medical device, and life sciences organizations in areas such as regulatory affairs, vigilance, risk management, and post‑market surveillance.
In the medical device domain, Wipro works with global manufacturers to ensure compliance with international regulatory frameworks including EU MDR, safety reporting standards, complaint handling systems, and quality management processes.
Professionals joining this role gain exposure to structured investigation workflows, global healthcare compliance standards, and cross‑functional collaboration within regulated environments.
Job Role & Responsibilities – Medical Device Investigator
The Medical Device Investigator will be responsible for evaluating product complaints, conducting safety investigations, and ensuring compliance with regulatory guidelines and internal quality systems.
Key Responsibilities
- Perform medical device complaint investigation and root cause analysis.
- Review product performance data and safety reports.
- Evaluate adverse events related to medical devices.
- Ensure compliance with EU MDR and global regulatory requirements.
- Prepare investigation reports with accurate clinical and technical documentation.
- Collaborate with cross‑functional stakeholders including quality, regulatory, and engineering teams.
- Maintain proper documentation aligned with regulatory and audit requirements.
- Ensure timely closure of investigations within defined service level agreements.
For experienced professionals, the role requires strong knowledge of medical device investigation processes, regulatory frameworks, and documentation standards.
For freshers, structured onboarding and training will support development in device safety analysis and investigation methodologies.
Eligibility & Qualifications
Educational Qualifications (Freshers & Experienced)
Eligible qualifications include:
B.Pharm, M.Pharm, Biomedical Engineering, Mechanical Engineering, BSc Medical Imaging & Radiology Technology, MSc Molecular Biology, BSc Nursing, BDS, BSc Biology, BS Medical Technology, BS Occupational Therapy, BS Psychology, BS Optometry, BS Respiratory Therapy, BS Midwifery, Bachelor of Physiotherapy, BS Speech Language Pathology, BS Veterinary Medicine.
Only candidates with the above-mentioned qualifications are eligible to attend the walk‑in drive.
Experience Criteria
- Kolkata Drive: Freshers eligible.
- Hyderabad & Pune Drives: 3–5 years of experience in Medical Device Investigation required.
Required Skills
- Strong knowledge of medical device safety and investigation procedures.
- Understanding of EU MDR and regulatory compliance standards (for experienced roles).
- Excellent written and verbal communication in English.
- Ability to work in rotational shifts (Pune role).
- Strong analytical and documentation skills.
- Readiness to work from office.
Candidates who attended a Wipro interview in the last three months are not eligible.
Walk‑In Details – Kolkata (Freshers)
Role: Medical Device Investigator
Location: Kolkata
Walk‑In Dates: 23rd, 24th, 25th February 2026
Reporting Time: 10:00 AM – 12:00 PM
Documents Required: Updated CV and original government ID card
Address: Gate 1, Plot No. 8 & 9, Block DM, Sector V, Salt Lake, Kolkata, West Bengal 700091
Walk‑In Details – Hyderabad (Interview Location) | Job Location Pune
Interview Location: Hyderabad
Work Location: Pune (Work From Office)
Walk‑In Dates: 25th & 26th February 2026
Reporting Time: 10:00 AM – 12:00 PM (No entry after 12:30 PM)
Contact Person: Pavan
Address: Wipro Limited, Survey No. 203/1, STPI Tower 6, 3rd Floor, Manikonda Village, Gachibowli, Hyderabad 500032
Experience Required: 3–5 years in Medical Device Investigation.
Walk‑In Details – Pune (Experienced Candidates)
Location: Pune (Work From Office)
Walk‑In Dates: 23rd & 24th February 2026
Reporting Time: 10:00 AM – 12:00 PM
Contact Person: Riya / Varsha
Address: Unit 2, Plot No 31, Hinjewadi Phase 2, Rajiv Gandhi Info Tech Park, Pune, Maharashtra 411057
Candidates must be ready for rotational shifts and possess strong knowledge of medical device investigation processes.
Why This Role Matters in Medical Device Compliance
Medical device investigation is a critical function within healthcare compliance and patient safety. With increasing regulatory scrutiny under EU MDR and global post‑market surveillance regulations, organizations require skilled investigators who can assess complaints, analyze adverse events, and ensure timely regulatory reporting.
This role contributes directly to patient safety, product quality assurance, and regulatory compliance across global markets. Professionals in this domain build expertise in risk management, clinical evaluation, and regulatory documentation.
Career Growth Opportunities
With experience, professionals can progress into:
- Senior Medical Device Investigator
- Post‑Market Surveillance Specialist
- Regulatory Affairs Associate
- Medical Safety Reviewer
- Quality & Compliance Manager
The medical device industry continues to grow rapidly, driven by regulatory changes and increasing global healthcare demand.
Frequently Asked Questions (FAQs)
1. Are freshers eligible?
Yes, freshers can attend the Kolkata walk‑in drive.
2. Is experience mandatory for Hyderabad and Pune drives?
Yes, 3–5 years of medical device investigation experience is required.
3. What documents should be carried?
Updated CV and original government ID card.
4. Is rotational shift mandatory?
Yes, candidates applying for the Pune role must be ready for rotational shifts.
5. Can candidates with other qualifications attend?
No, only the specified qualifications are eligible.
Summary Table
| Company | Wipro |
| Vacancies | Medical Device Investigator (Freshers & Experienced) |
| Required Education | B.Pharm, M.Pharm, Biomedical/Mechanical Engineering, BSc Medical Imaging, MSc Molecular Biology, Nursing, BDS, Allied Health Sciences |
| Experience | Freshers (Kolkata); 3–5 years Medical Device Investigation (Hyderabad & Pune) |
