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Wipro Hiring Medical Device Complaint Investigators – Pune, Kolkata & Hyderabad

Published on

Wipro

Any Life Science Graduate, B.Pharm, M.Pharm, Biomedical Engineering, Mechanical Engineering, B.Sc Nursing, Biology, Medical Technology, BDS, Physiotherapy, Psychology, Optometry, Radiology, Respiratory Therapy, Veterinary Medicine

Pune, Kolkata & Hyderabad

0 - 9 Years

Verified Job

Walk In Interview
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Wipro Limited has announced multiple openings for Medical Device Complaint Investigator roles across Pune and Kolkata, with walk-in interviews scheduled in Pune, Kolkata, and Hyderabad.

⚠️ Important Note for Candidates:
The Hyderabad walk-in drive is strictly for experienced professionals (3 to 9 years) in medical device complaint investigation, risk management, and CAPA. Freshers are NOT eligible for the Hyderabad interview.

This hiring drive is highly relevant for professionals working in Medical Devices, PMS, EU MDR, ISO 13485, and ISO 14971 risk management domains, looking for immediate joining opportunities with a global organization.

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Job Overview

  • Company: Wipro Limited
  • Job Title: Medical Device Complaint Investigator
  • Domain: Medical Devices | Regulatory Affairs | Post-Market Surveillance
  • Job Locations:
    • Pune (Primary)
    • Kolkata
  • Interview Locations: Pune, Kolkata, Hyderabad
  • Work Mode: Work From Office (WFO)
  • Shift: Rotational / Fixed Night Shift (role & location dependent)

Critical Clarification – Experience Requirement by Location

Hyderabad Walk-In

  • Experience Required: 3 to 9 years ONLY
  • Freshers are NOT eligible
  • Interview is conducted in Hyderabad, but
    Job Location will be Pune (WFO)

Pune & Kolkata Walk-In

  • Experience Range:
    • Pune: 0 to 9 years
    • Kolkata: 0 to 5 years (relevant experience preferred)

Key Roles & Responsibilities (In-Depth)

Selected candidates will be responsible for end-to-end medical device complaint investigation activities, including:

  • Perform comprehensive complaint investigations as per global regulatory requirements
  • Conduct risk analysis and risk evaluation using ISO 14971 methodologies
  • Apply FMEA tools for hazard identification and risk control assessment
  • Support CAPA investigations, root cause analysis, and effectiveness checks
  • Ensure compliance with ISO 13485 Quality Management System
  • Work on Post-Market Surveillance (PMS) and trending activities
  • Support EU MDR complaint handling and vigilance requirements
  • Prepare clear, concise, and compliant investigation reports
  • Collaborate with global stakeholders, QA, RA, and engineering teams
  • Maintain audit-ready documentation aligned with regulatory expectations

👉 For Hyderabad candidates, hands-on experience in the above activities is mandatory.


Eligibility & Qualification Criteria

Educational Qualification

  • Any Life Science Graduate
  • B.Pharm / M.Pharm
  • Biomedical / Mechanical Engineering
  • B.Sc Nursing, Biology, Medical Technology
  • BDS, Physiotherapy, Psychology, Optometry
  • Radiology, Respiratory Therapy, Veterinary Medicine (Kolkata drive)

⚠️ Only the mentioned qualifications are eligible


Experience Requirements (Very Important)

Hyderabad Walk-In

  • 3–9 years of relevant experience
  • Mandatory experience in:
    • Medical Device Complaint Investigation
    • Risk Management & CAPA
    • ISO 13485 & ISO 14971 compliance

Pune & Kolkata

  • Freshers to experienced candidates may apply
  • Prior medical device investigation experience is an advantage

Mandatory Skills

  • Excellent written and verbal English communication
  • Strong understanding of medical device lifecycle
  • Knowledge of EU MDR, PMS, Vigilance, Risk Management
  • Ability to work in rotational or night shifts
  • Willingness to relocate and work from office
  • Immediate joiners only

Walk-In Interview Details

Hyderabad Walk-In (Experienced Only)

  • Date: 4 February 2026
  • Time: 10:00 AM – 12:30 PM
  • Interview Location:
    Wipro Limited, Manikonda STPI,
    Survey No. 203/1, Tower 6, 3rd Floor,
    Gachibowli, Hyderabad – 500032
  • Job Location: Pune (WFO)
  • Contact Person: Pavan

Pune Walk-In

  • Dates: 3 & 6 February 2026
  • Time: 10:00 AM – 12:30 PM
  • Venue:
    Unit 2, Plot No. 31,
    Hinjewadi Phase 2, Rajiv Gandhi Infotech Park,
    Pune – 411057
  • Contacts: Riya / Varsha

Kolkata Walk-In

  • Dates: 2 & 5 February 2026
  • Time: 10:00 AM – 12:00 PM
  • Shift: Fixed Night Shift
  • Venue:
    Gate 1, Plot No. 8 & 9, Block DM,
    Sector V, Salt Lake, Kolkata – 700091
  • Contact: Sarita

Documents Required

  • Updated Resume
  • Original Government ID Proof
  • Mention “Source of Walk-In Information” at the top of your CV

Salary Range (Indicative)

  • ₹4.5 LPA to ₹12 LPA, depending on:
    • Experience
    • Domain expertise
    • Interview performance

Why Experienced Professionals Should Consider Wipro

  • Exposure to global medical device clients
  • Strong focus on EU MDR & international compliance
  • Stable long-term projects in PMS & Complaint Handling
  • Clear career progression in Regulatory & Quality domains
  • High demand skillset for future leadership roles

Email Application Option

Candidates who cannot attend walk-ins may share their resume to:
📧 merlin.michael@wipro.com

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