Enovis is hiring a Post Market Surveillance & Vigilance Specialist for its Surgical International team in Hyderabad, Telangana. The position is listed as a full-time, full-remote opportunity and focuses on global post-market surveillance, vigilance, complaint handling, regulatory reporting, trend monitoring and PMS data analysis.
The role is suited to professionals with 1–3 years of experience in the medical device or healthcare industry, particularly candidates with exposure to complaint handling, vigilance, regulatory affairs, quality systems or post-market surveillance.
The position will work closely with Regulatory Affairs, Quality, Clinical Affairs, Risk Management, R&D, Manufacturing and local affiliate teams to support patient safety, regulatory compliance and continuous product improvement.
Enovis Post Market Surveillance Specialist Job Details
| Job Details | Information |
|---|---|
| Company | Enovis |
| Job Title | Post Market Surveillance & Vigilance Specialist |
| Department | Regulatory Affairs – Surgical International |
| Location | Hyderabad, Telangana, India |
| Work Mode | Full Remote |
| Employment Type | Full Time |
| Experience | 1–3 Years |
| Job Requisition ID | R0032454 |
| Posted | September 23, 2026 |
| Application | Enovis Careers |
The original job listing identifies Hyderabad as the location, full-time employment and requisition R0032454.
About Enovis
Enovis is a global medical technology company focused on clinically differentiated solutions designed to improve patient outcomes and transform healthcare workflows. The company operates across medical technology and orthopedics and emphasizes continuous improvement, innovation and collaboration.
For candidates looking for medical device jobs, regulatory affairs jobs and post-market surveillance careers, this position provides exposure to global vigilance and post-market activities.
Post Market Surveillance Specialist Responsibilities
The selected candidate will support global post-market surveillance and vigilance activities for medical devices marketed worldwide.
Complaint Handling and Triage
Key responsibilities include:
- Performing intake, review, assessment and data entry of product complaints.
- Evaluating complaint completeness and requesting additional information where required.
- Performing initial complaint triage and categorization according to established procedures.
- Supporting complaint review and follow-up activities.
- Maintaining accurate and complete complaint records in accordance with quality and regulatory requirements.
Regulatory Reporting
The Post Market Surveillance Specialist will also:
- Prepare and maintain vigilance and adverse-event reports for regulatory authorities worldwide.
- Ensure regulatory submissions are complete, accurate and submitted within required timelines.
- Maintain documentation supporting regulatory reporting decisions and communications.
PMS Data Management and Analysis
Responsibilities include:
- Collecting, consolidating and analyzing post-market surveillance data from multiple sources.
- Generating PMS metrics, dashboards and periodic reports.
- Supporting PMS Reports, Periodic Safety Update Reports (PSURs) and other post-market deliverables.
- Monitoring data quality and identifying process-improvement opportunities.
- Supporting benefit-risk evaluation activities through data collection and analysis.
- Participating in proactive PMS activities to identify emerging risks and opportunities for product improvement.
- Performing complaint trending and statistical evaluations to identify potential safety signals.
- Supporting escalation of adverse trends requiring further investigation.
- Collaborating with cross-functional teams on trend-analysis outcomes.
- Supporting Health Hazard Evaluation activities through data gathering, analysis and documentation.
Quality Systems and Process Improvement
The role will also support the revision and maintenance of PMS & Vigilance SOPs, Work Instructions and associated forms.
Enovis Post Market Surveillance Specialist Qualifications
Candidates should have a Bachelor’s degree in one of the following areas:
- Biomedical Engineering
- Life Sciences
- Pharmacy
- Biotechnology
- Quality
- Regulatory Affairs
- Related scientific disciplines
Advanced degrees are considered an advantage.
Experience Required
Enovis is seeking candidates with:
- 1–3 years of experience in the medical device or healthcare industry.
- Previous experience in complaint handling, vigilance, regulatory affairs, quality systems or post-market surveillance is preferred.
Technical Knowledge and Skills
Familiarity with the following areas is advantageous:
- EU MDR
- FDA Medical Device Reporting requirements
- ISO 13485
- Post-Market Surveillance principles
- Complaint handling processes
- Vigilance reporting requirements
- Agile PLM
- Complaint management databases
- Power BI
- Microsoft Excel
The job description also emphasizes analytical and problem-solving abilities, attention to detail, data accuracy, written and verbal English communication, remote working capability, organization, prioritization and cross-functional collaboration.
Enovis Job Benefits
The supplied job description states that the benefits package includes:
- Medical insurance
- Life insurance
- Accidental insurance
- Leaves
- Holidays
Enovis’ current careers information also describes health and wellness benefits, time-off benefits, financial-wellbeing programs, parental leave and flexible working arrangements across its global workforce.
How to Apply
