Wipro walk-in Medical Device Complaint Investigator

Life Science Complaint Investigator Vacancies – Wipro Pune

Life science graduate complaint investigator vacancies at Wipro Pune. Freshers to 9 years experience, walk-in interview.

Wipro has announced a walk-in interview drive for Medical Device Complaint Investigator roles at its Pune location. This hiring initiative targets life sciences graduates ranging from freshers to experienced professionals who want to build or advance their careers in the fast-growing medical devices and healthcare compliance domain. The role offers exposure to global regulatory standards, risk management systems, and real-world complaint investigation processes within a structured corporate environment.

Company Overview

Wipro Limited is a globally recognized technology and services company with a strong presence in healthcare, life sciences, and medical devices services. Through its healthcare and medical device verticals, Wipro supports global manufacturers in meeting regulatory, quality, and compliance requirements across regulated markets.

Wipro’s medical device and healthcare quality teams work closely with international clients to ensure patient safety, regulatory adherence, and product reliability. The organization follows globally accepted standards such as ISO 13485, ISO 14971, and FDA Quality System Regulations, making it an ideal workplace for professionals aiming to build expertise in medical device risk management and complaint investigation.

Job Role & Responsibilities

Designation: Medical Device Complaint Investigator

Work Mode: Work From Office (WFO)

The Medical Device Complaint Investigator plays a critical role in evaluating, documenting, and resolving customer complaints related to medical devices. This position directly contributes to patient safety, regulatory compliance, and continuous product improvement.

Key responsibilities include:

• Investigating medical device complaints in accordance with regulatory requirements
• Performing root cause analysis using risk management tools such as FMEA
• Conducting risk assessments aligned with ISO 14971 guidelines
• Managing CAPA activities and ensuring timely closure
• Reviewing complaint data for trends and potential safety signals
• Preparing detailed investigation reports with strong technical write-ups
• Ensuring compliance with ISO 13485 and applicable regulatory standards
• Collaborating with cross-functional teams for complaint resolution
• Maintaining accurate documentation and audit-ready records

This role provides valuable exposure to global medical device regulations and quality systems, making it highly relevant for long-term careers in medical device quality, vigilance, and regulatory compliance.

Eligibility / Qualifications

Educational Qualification

Any Life Science Graduate

Relevant courses include:

BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biomedical Sciences, BPharm, MPharm, MSc Life Sciences, MSc Biotechnology, MSc Microbiology

Experience Requirement

• 0 to 9 years of experience
• Freshers with strong understanding of medical device quality concepts can apply
• Immediate joiners are strongly preferred

Skills & Competencies

• Strong communication skills in English
• Knowledge of medical device complaint handling processes
• Understanding of risk management, CAPA, and investigation methodologies
• Familiarity with ISO 13485 and ISO 14971 standards
• Willingness to work rotational shifts
• Readiness to relocate to Pune and work from office

Location & Salary

Job Location

Pune, Maharashtra (Work From Office)

Interview Location

Unit 2, Plot No. 31
Hinjewadi Phase 2
Rajiv Gandhi Infotech Park
Pune, Maharashtra – 411057

Salary details are not disclosed and will be offered based on experience, skill set, and internal compensation structures.

Walk-In Interview Details

Walk-In Dates

03 February 2026 and 06 February 2026

Reporting Time

10:00 AM to 12:30 PM

Candidates are advised to report within the specified time window for smooth interview processing.

Application Process

Eligible candidates can attend the walk-in interview directly at the venue.

Documents to Carry

• Updated resume
• Original government-issued ID card

Candidates must clearly mention the source of information about the walk-in interview at the top of their CV.

Contact Persons

Riya / Varsha

Why Build Your Medical Device Career with Wipro

• Exposure to global medical device clients and regulatory standards
• Strong learning curve in complaint investigation and risk management
• Opportunity to work with ISO and FDA-aligned quality systems
• Stable corporate environment with long-term growth prospects
• Direct contribution to patient safety and healthcare quality

Frequently Asked Questions (FAQs)

Who can attend this Wipro walk-in interview?

Life science graduates with 0 to 9 years of experience can attend the walk-in.

Are freshers eligible for this role?

Yes. Freshers with relevant knowledge of medical device quality systems can apply.

Is this a work-from-home role?

No. This is a work-from-office role based in Pune.

Are immediate joiners mandatory?

Immediate joiners are strongly preferred for this hiring drive.

SEO Title Variations for Higher Visibility

• Wipro Walk-In for Medical Device Complaint Investigator Pune
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Summary Table

Category	Details
Company	Wipro Limited
Vacancies	Medical Device Complaint Investigator
Required Education	Life Science Graduates
Experience	0 to 9 Years