Medical Device Complaint Investigator

Published on

Wipro

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πŸŽ“ Medical
πŸ“ Pune
πŸ’Ό 3 - 8 years
βœ” Verified Job
Email Application
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Wipro is hiring Medical Device Complaint Investigators to support global medical device quality and regulatory operations. The role involves complaint investigation, complaint assessment, risk management, CAPA activities, regulatory compliance, and quality documentation. Selected candidates will work with international healthcare clients while gaining practical experience with ISO quality standards and medical device vigilance processes. This is an excellent opportunity to build a long-term career in Medical Device Quality, Regulatory Affairs, and Healthcare Technology.

Job Overview

Particulars Details
Position Medical Device Complaint Investigator
Company Wipro
Location Pune
Job Type Full-Time
Experience 3 - 8 years
Category / Department Medical
Application Mode Email

🏒 About Wipro

Wipro is a leading global technology services and consulting company delivering innovative solutions across healthcare, life sciences, engineering, digital transformation, and enterprise technologies.

Company Mission

To help organizations transform through technology, innovation, and customer-focused solutions while delivering sustainable business value.

Company Vision

To be a trusted global partner that enables businesses and communities to thrive through innovation and digital excellence.

Core Values

β€’ Integrity
β€’ Excellence
β€’ Innovation
β€’ Respect
β€’ Customer Focus
β€’ Collaboration
β€’ Continuous Learning

What Makes Them Different

Wipro combines global technology expertise with healthcare and life sciences capabilities, providing professionals with opportunities to work on high-impact international projects.

Leadership/Company Philosophy

The organization encourages innovation, diversity, ethical practices, continuous learning, and professional growth through a collaborative work culture.

πŸ’‘ Editor's Note / Preparation Tip

πŸ“„ Resume Preparation Tips

β€’ Highlight experience in Medical Devices, Pharmacovigilance, or Quality Assurance.
β€’ Mention knowledge of ISO 13485, ISO 14971, CAPA, and Risk Management.
β€’ Include documentation and investigation experience.
β€’ Showcase analytical, communication, and teamwork skills.
β€’ Optimize your resume using ATS-friendly healthcare and medical device keywords.

🎯 Interview Preparation

β€’ Revise Medical Device Complaint Investigation concepts.
β€’ Understand CAPA, Risk Management, and complaint handling workflows.
β€’ Review ISO 13485 and ISO 14971 standards.
β€’ Prepare examples demonstrating analytical thinking and quality compliance.
β€’ Practice communication and scenario-based interview questions.

πŸ’‘ Professional Tips

β€’ Stay updated with global Medical Device regulations.
β€’ Strengthen quality documentation and investigation skills.
β€’ Learn root cause analysis methodologies.
β€’ Develop expertise in regulatory compliance and quality systems.
β€’ Continue building knowledge in Medical Device Vigilance and Healthcare Quality.

πŸ“ Job Description

πŸš€ Medical Device Complaint Investigator Hiring | Wipro

Looking to build or advance your career in Medical Device Complaint Investigation? Wipro is conducting a Walk-In Drive for Medical Device Complaint Investigator roles for candidates with 0–8 years of experience. This is an excellent opportunity for Pharmacy, Biomedical Engineering, Nursing, and Life Sciences professionals to work with a global organization and gain hands-on experience in Medical Device Vigilance, Risk Management, CAPA, and international quality standards.

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πŸ“Œ Position Details
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πŸ’Ό Position: Medical Device Complaint Investigator
🏒 Company: Wipro
πŸ“ Work Location: Pune, Maharashtra
πŸ“ Interview Locations: Pune, Hyderabad & Gurgaon
🏒 Work Mode: Work From Office (WFO)
πŸ’Ό Experience: 0–8 Years (Pune Walk-In: 3–8 Years)
πŸŽ“ Qualification: B.Pharm, M.Pharm, Pharm.D, Biomedical Engineering, Nursing, B.Sc. Life Sciences, M.Sc. Life Sciences, or other relevant Life Sciences degrees
πŸ“„ Employment Type: Full-Time
πŸ’° Salary: β‚Ή4 – β‚Ή18 LPA (Based on Experience & Company Norms)
πŸ“… Walk-In Dates: 8 July 2026 – 10 July 2026
πŸ•™ Reporting Time: 10:00 AM – 12:00 PM
⚑ Joining Preference: Immediate Joiners Preferred

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⭐ Preferred Skills
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⭐ Experience in Medical Device Complaint Handling
⭐ Understanding of Medical Device Regulations
⭐ Strong documentation and reporting skills
⭐ Good analytical and problem-solving abilities
⭐ Ability to work in a fast-paced environment
⭐ Professional communication skills
⭐ Immediate availability to join

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πŸŽ“ Candidate Requirements
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β€’ B.Pharm, M.Pharm, Pharm.D, Biomedical Engineering, Nursing, B.Sc. Life Sciences, M.Sc. Life Sciences, or equivalent Life Sciences qualification.
β€’ Hyderabad & Gurgaon Walk-In: 0–8 Years of experience.
β€’ Pune Walk-In: 3–8 Years of experience.
β€’ Strong English communication skills.
β€’ Knowledge of Medical Device Complaint Investigation, Risk Management, CAPA, ISO 14971, and ISO 13485.
β€’ Willingness to work rotational shifts.
β€’ Candidates attending Hyderabad or Gurgaon interviews should be willing to relocate to Pune.

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🌟 Why Join Wipro?
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βœ” Join one of the world’s leading technology and healthcare service organizations.
βœ” Build expertise in Medical Device Complaint Investigation.
βœ” Gain exposure to international Medical Device Quality Systems.
βœ” Work with ISO 13485 and ISO 14971 standards.
βœ” Career growth in Medical Device Quality and Regulatory Affairs.
βœ” Continuous learning and professional development opportunities.
βœ” Collaborate with global healthcare and medical device clients.

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πŸ“ Walk-In Interview Venues
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πŸ“ Pune Interview Venue
Unit 2, Plot No. 31
Hinjewadi Phase 2
Rajiv Gandhi Infotech Park
Pune – 411057

πŸ“ Hyderabad Interview Venue
Wipro Limited
Manikonda STPI
Survey No. 203/1
STPI Tower 6, 3rd Floor
Manikonda Village
Gachibowli
Hyderabad – 500032

πŸ“ Gurgaon Interview Venue
Wipro HR Services India Pvt. Ltd.
(SEZ) Building 2
Candor Techspace IT/ITES SEZ
Tikri, Sector 48
Gurgaon – 122001

πŸ“’ Know someone who would be a great fit? Tag them or share this opportunity with your network!


🎯 Key Responsibilities

  • βœ“ Investigate medical device complaints and document findings accurately.
  • βœ“ Perform complaint assessment and maintain complete investigation records.
  • βœ“ Support Risk Management activities and product safety evaluations.
  • βœ“ Participate in CAPA implementation and monitoring.
  • βœ“ Follow ISO 14971 risk management processes.
  • βœ“ Support compliance with ISO 13485 quality management systems.
  • βœ“ Maintain investigation reports and quality documentation.
  • βœ“ Collaborate with global quality and regulatory teams.
  • βœ“ Ensure compliance with company SOPs and quality standards.

πŸ’‘ Required Qualifications & Skills

βœ“ Medical Device Complaint Investigation βœ“ Complaint Assessment & Documentation βœ“ Risk Management βœ“ CAPA Knowledge βœ“ ISO 14971 Awareness βœ“ ISO 13485 Quality Systems βœ“ Regulatory Compliance βœ“ Quality Documentation βœ“ English Communication Skills βœ“ Analytical Thinking βœ“ Team Collaboration βœ“ Willingness to Work Rotational Shifts βœ“ Ready to Relocate to Pune (if applicable)

Frequently Asked Questions

Q1. Who can apply for this role?
βœ… Candidates with Pharmacy, Biomedical Engineering, Nursing, and Life Sciences qualifications.

Q2. Where will the selected candidates work?
βœ… The work location is Pune, Maharashtra.

Q3. Are freshers eligible?
βœ… Yes. Candidates with 0–8 years of experience can apply, while the Pune drive prefers candidates with 3–8 years of experience.

Q4. What documents should I bring for the walk-in?
βœ… Updated Resume/CV, Original Government Photo ID, and mention the source of the walk-in at the top of your CV.

Q5. Is relocation required?
βœ… Yes. Candidates attending interviews in Hyderabad or Gurgaon should be willing to relocate to Pune after selection.

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