Vantive Hiring Executive, Post Market Surveillance | Gurgaon
Vantive has announced a new opportunity for Executive, Post Market Surveillance at its Gurgaon office. This role is ideal for professionals interested in medical device vigilance, complaint handling, MDR reporting, quality assurance, and regulatory compliance.
Candidates looking to build careers in Medical Device Regulatory Affairs, Post Market Surveillance, Quality Systems, and Complaint Investigation functions are encouraged to apply.
📋 Job Overview
| Details | Information |
|---|---|
| Position | Executive, Post Market Surveillance |
| Company | Vantive |
| Location | Gurgaon, Haryana |
| Job Type | Full-Time |
| Department | Quality & Regulatory Affairs |
| Industry | Medical Devices / Healthcare |
| Job ID | JR-194925 |
🏢 About Vantive
Vantive is a dedicated vital organ therapy company focused on extending lives and expanding possibilities for patients worldwide.
Building on more than 70 years of innovation in kidney care, Vantive develops advanced therapies, digital healthcare solutions, and patient-focused technologies that improve outcomes globally.
📌 Key Responsibilities
- Evaluate product quality complaints and initiate quality system actions.
- Own and process complaints according to company procedures.
- Perform complaint investigations and ensure timely closure.
- Conduct reportability assessments for adverse events and complaints.
- Prepare Medical Device Reports (MDR).
- Prepare Manufacturer Incident Reports (MIR).
- Support global regulatory submissions.
- Monitor investigations and coordinate with cross-functional teams.
- Review findings from Engineering, Manufacturing, QA, Service Teams, and Suppliers.
- Perform complaint trend analysis and quality metric reporting.
- Support continuous improvement initiatives.
- Ensure compliance with Quality Management Systems.
🎓 Educational Requirements
- Bachelor's Degree in Pharmacy
- Life Sciences
- Biomedical Engineering
- Biotechnology
- Medical Devices
- Related Healthcare Disciplines
⭐ Preferred Experience & Skills
- Post Market Surveillance (PMS)
- Medical Device Vigilance
- Complaint Handling
- Quality Assurance
- Regulatory Affairs
- Medical Device Reporting
- MDR Regulations
- MIR Reporting
- FDA Quality System Requirements
- ISO 13485
- Risk Management Processes
- Strong Analytical Skills
- Communication Skills
🚀 Why Join Vantive?
- Work with a global healthcare innovator.
- Exposure to international medical device regulations.
- Career growth in Quality and Regulatory Affairs.
- Patient-focused and collaborative culture.
- Contribute to life-saving healthcare technologies.
- Global learning and development opportunities.
📈 Career Scope in Post Market Surveillance
Post Market Surveillance professionals play a critical role in ensuring patient safety and regulatory compliance across medical device organizations.
Experience in this field can lead to careers such as Medical Device Vigilance Specialist, Regulatory Affairs Specialist, Complaint Handling Specialist, Quality Systems Engineer, Clinical Safety Associate, and Global Regulatory Affairs Executive.
📄 ATS-Friendly Resume Tips
- Add keywords such as PMS, MDR, MIR, Medical Device Vigilance, Complaint Handling, Regulatory Affairs, ISO 13485, and Quality Systems.
- Highlight complaint investigations and regulatory reporting experience.
- Mention CAPA, Risk Management, and Quality System knowledge.
- Use measurable achievements where possible.
- Keep resume ATS-friendly and professionally structured.
💡 Interview Preparation Tips
- Review MDR and MIR reporting concepts.
- Understand complaint handling workflows.
- Revise ISO 13485 and FDA Quality System requirements.
- Prepare examples of investigations and quality improvement initiatives.
- Understand Post Market Surveillance processes.
📝 How to Apply
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Complete the countdown timer below.
- Apply through the official Vantive Careers portal.
🚀 Job Application Link
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
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