Vantive, a global leader in kidney care and vital organ therapy solutions, has announced a new opportunity for the position of Executive, Post Market Surveillance at its Gurgaon, Haryana location. This role is ideal for professionals with experience in medical device vigilance, complaint handling, MDR reporting, post-market surveillance, quality systems, and regulatory compliance.
Candidates looking to build a career in medical device regulatory affairs, quality assurance, complaint management, and post-market surveillance jobs in India should consider applying for this position.
About Vantive
Vantive is a dedicated vital organ therapy company focused on extending lives and expanding possibilities for patients worldwide. Building on a 70-year legacy in kidney care innovation, the company continues to develop advanced therapies, digital healthcare solutions, and patient-focused technologies.
The organization offers employees the opportunity to work on life-saving products while contributing to global healthcare innovation.
Job Details
| Particulars | Details |
|---|---|
| Position | Executive, Post Market Surveillance |
| Company | Vantive |
| Location | Gurgaon, Haryana, India |
| Job Type | Full-Time |
| Department | Quality & Regulatory Affairs |
| Industry | Medical Devices / Healthcare |
| Job ID | JR – 194925 |
Key Responsibilities
The selected candidate will be responsible for:
- Evaluating potential product quality complaints and initiating appropriate quality system actions.
- Owning and processing product complaints according to company procedures.
- Performing complaint investigations and ensuring timely closure.
- Conducting reportability assessments for adverse events and product complaints.
- Preparing and submitting regulatory reports including:
- Medical Device Reports (MDR)
- Manufacturer Incident Reports (MIR)
- Other applicable global regulatory submissions
- Monitoring complaint investigations and coordinating with cross-functional teams.
- Reviewing investigation findings from:
- Engineering
- Manufacturing
- Quality Assurance
- Service Teams
- Suppliers
- Performing complaint trend analysis and generating quality metrics.
- Supporting continuous improvement initiatives within the Post Market Surveillance function.
- Ensuring compliance with applicable quality management system requirements.
Required Qualifications
Candidates with the following qualifications are encouraged to apply:
Educational Requirements
- Bachelor’s Degree in:
- Pharmacy
- Life Sciences
- Biomedical Engineering
- Biotechnology
- Medical Devices
- Related Healthcare Discipline
Preferred Experience
- Experience in:
- Post Market Surveillance (PMS)
- Medical Device Vigilance
- Complaint Handling
- Quality Assurance
- Regulatory Affairs
- Medical Device Reporting
- Understanding of:
- MDR Regulations
- MIR Reporting
- FDA Quality System Requirements
- ISO 13485
- Risk Management Processes
- Strong analytical and communication skills.
Why Join Vantive?
Working at Vantive offers several benefits:
- Opportunity to work with a global healthcare innovator.
- Exposure to international medical device regulations.
- Career growth in quality and regulatory affairs.
- Collaborative and patient-focused work culture.
- Involvement in life-saving healthcare technologies.
- Global learning and development opportunities.
Career Scope of Post Market Surveillance Professionals
Post Market Surveillance professionals play a critical role in ensuring patient safety and regulatory compliance. Experience in this field can open career opportunities such as:
- Medical Device Vigilance Specialist
- Regulatory Affairs Specialist
- Complaint Handling Specialist
- Quality Systems Engineer
- Clinical Safety Associate
- Global Regulatory Affairs Executive
- Medical Device Compliance Manager
With increasing regulatory requirements worldwide, demand for professionals in post market surveillance jobs, medical device vigilance careers, MDR reporting jobs, and quality complaint investigation roles continues to grow.
How to Apply
