Wipro Hiring Medical Device Complaint Investigator
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirement
- Skill Requirements
- Eligible Courses (Comma-Separated)
- Location & Salary
- Interview Location
- Job Location
- Work Model
- Salary Information
- Application Process
- Walk-in Details
- Documents to Carry
- FAQs
- Who can attend this walk-in interview?
- Is this role open to freshers?
- Where is the job location?
- Are rotational shifts mandatory?
- Is relocation to Pune required?
- Summary Table
Wipro is organizing a walk-in interview for experienced professionals for the role of Medical Device Complaint Investigator. This hiring drive is aimed at candidates with strong backgrounds in medical device complaint investigation, risk assessment, and CAPA management. Multiple vacancies are available under the medical device quality and compliance function. The interview will be conducted in Hyderabad on 13 February 2026, while the job location will be Pune, Maharashtra, with a full work-from-office model. This opportunity is strictly for experienced professionals with 3–9 years of relevant experience who are available to join immediately.
Company Overview
Wipro is a global technology and services organization with a well-established healthcare and medical device services vertical. Through its life sciences and medical device operations, Wipro supports global manufacturers in post-market surveillance, complaint investigation, risk management, and regulatory compliance activities aligned with international standards.
Wipro’s medical device teams work closely with global clients to ensure patient safety, product quality, and regulatory adherence across the device lifecycle. The organization follows structured quality systems aligned with ISO 13485, ISO 14971, and global regulatory expectations. For experienced professionals, Wipro offers exposure to complex investigations, global compliance programs, and long-term career growth in medical device quality and risk management domains.
Job Role & Responsibilities
The Medical Device Complaint Investigator role focuses on investigating device-related complaints and supporting risk management activities for regulated medical device products. The position requires in-depth knowledge of investigation methodologies, documentation standards, and quality system requirements.
Key Responsibilities
- Performing detailed medical device complaint investigations in accordance with approved procedures
- Conducting risk assessments and failure mode evaluations related to device complaints
- Supporting CAPA initiation, documentation, and follow-up activities
- Reviewing complaint data, investigation findings, and supporting evidence
- Documenting investigation outcomes clearly within defined timelines
- Supporting complaint trending, escalation, and root cause analysis activities
- Ensuring compliance with internal quality systems and regulatory standards
- Collaborating with quality, regulatory, and cross-functional teams
- Maintaining accurate documentation and data integrity across systems
These responsibilities directly support patient safety, regulatory compliance, and continuous improvement initiatives for medical device products.
Eligibility / Qualifications
Educational Qualification
- Any Life Science Graduate
Experience Requirement
- 3 to 9 years of relevant experience in medical device complaint investigation
- Immediate joiners only
Skill Requirements
- Extensive knowledge of medical device risk management principles
- Hands-on experience with CAPA processes and complaint investigation
- Strong understanding of investigation workflows and documentation
- Excellent verbal and written communication skills in English
- Willingness to work rotational shifts
- Readiness to relocate to Pune and work from office
- Ability to manage complex cases under tight timelines
Eligible Courses (Comma-Separated)
BSc Life Sciences, MSc Life Sciences, BSc Biotechnology, MSc Biotechnology, B.Pharm, M.Pharm, Biomedical Engineering
Location & Salary
Interview Location
Hyderabad, Telangana, India
Job Location
Pune, Maharashtra, India
Work Model
Full-time | Work from Office | Rotational Shifts
Salary Information
Salary will be offered as per industry standards and will depend on experience, skill depth, and role fitment. The role offers exposure to global medical device programs, advanced investigation practices, and structured quality systems.
Application Process
Interested and eligible candidates must attend the walk-in interview in person on the scheduled date. No prior online application is required.
Walk-in Details
- Walk-in Date: 13 February 2026
- Reporting Time: 10:00 AM – 12:30 PM
- Venue: Wipro Limited, Manikonda STPI, Survey No. 203/1, STPI, Tower 6, 3rd Floor, Manikonda Village, Gachibowli, Hyderabad – 500032
- Contact Person: Pavan
Documents to Carry
- Updated CV (mention the source of walk-in information at the top)
- Original Government-issued ID card
Candidates are advised to attend the interview only if they meet the experience and immediate joining criteria.
FAQs
Who can attend this walk-in interview?
Candidates with 3–9 years of experience in medical device complaint investigation and risk management can attend.
Is this role open to freshers?
No. This role is strictly for experienced professionals.
Where is the job location?
The job location is Pune, Maharashtra, while the interview will be conducted in Hyderabad.
Are rotational shifts mandatory?
Yes. Candidates must be willing to work rotational shifts.
Is relocation to Pune required?
Yes. Selected candidates must be ready to relocate to Pune and work from office.
Summary Table
| Company | Wipro |
|---|---|
| Vacancies | Medical Device Complaint Investigator |
| Required Education | Life Science Graduates, Pharmacy, Biomedical Engineering |
| Experience | 3–9 Years (Immediate Joiners) |
