If you are looking for Executive, Post Market Surveillance jobs in Gurgaon, medical device vigilance jobs, or post market surveillance careers in India, Vantive has announced an exciting full-time opportunity for professionals interested in complaint handling, regulatory reporting, and medical device safety.
This Executive, Post Market Surveillance position is based in Gurgaon, Haryana and offers the opportunity to work with one of the world’s leading organizations dedicated to advancing kidney care and vital organ therapies. Candidates with backgrounds in Pharmacy, Life Sciences, Biomedical Engineering, or related healthcare disciplines will find this role particularly suitable.
About Vantive
Vantive is a global healthcare company focused on transforming kidney care and expanding therapies for vital organs. With more than 70 years of innovation, the company develops advanced dialysis technologies, digital healthcare solutions, and patient-centered therapies designed to improve outcomes worldwide.
Working at Vantive provides exposure to global medical device regulations, post-market surveillance, complaint management, and regulatory compliance.
Job Details
| Particular | Details |
|---|---|
| Company | Vantive |
| Job Title | Executive, Post Market Surveillance |
| Location | Gurgaon, Haryana, India |
| Employment Type | Full-Time |
| Department | Post Market Surveillance |
| Experience | 0โ3 Years (Preferred) |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biomedical Engineering, Biotechnology or related healthcare discipline |
| Industry | Medical Devices / Healthcare / Pharmacovigilance |
Key Responsibilities
The selected candidate will be responsible for:
- Managing customer complaints for medical devices.
- Opening and documenting complaint records accurately.
- Collecting complete complaint information from customers.
- Conducting written and verbal customer follow-ups.
- Assessing complaint reportability under applicable regulations.
- Preparing Medical Device Reports (MDRs).
- Coordinating complaint investigations and sample retrieval.
- Responding to customer queries professionally.
- Closing complaint cases within established timelines.
- Managing complaint workflow and escalating critical issues.
- Triaging internal and external complaint communications.
- Supporting continuous improvement initiatives.
- Maintaining regulatory compliance and documentation standards.
Required Qualifications
Candidates should preferably possess:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biomedical Engineering
- Biotechnology
- Other relevant healthcare or life sciences qualifications
Preferred Skills
Successful candidates should have:
- Medical device vigilance knowledge
- Post Market Surveillance understanding
- Complaint handling experience
- Medical Device Reporting (MDR)
- Regulatory documentation
- Strong written and verbal communication
- Analytical thinking
- Customer interaction skills
- Attention to detail
- Time management
- Microsoft Office proficiency
- Ability to work in cross-functional teams
Salary
Based on similar medical device surveillance roles in Gurgaon, the estimated salary is:
โน4.8 LPA โ โน7.5 LPA (CTC)
Actual compensation may vary depending on qualifications and experience.
Benefits
Employees at Vantive may receive:
- Competitive salary package
- Health and medical insurance
- Global work environment
- Career development opportunities
- Learning and training programs
- Exposure to international regulatory processes
- Inclusive workplace culture
- Employee wellness initiatives
- Performance-based growth opportunities
Why Join Vantive?
This opportunity is ideal for professionals seeking careers in:
- Post Market Surveillance Jobs
- Medical Device Safety Jobs
- Medical Device Vigilance Careers
- Pharmacovigilance Jobs
- Complaint Handling Jobs
- MDR Specialist Jobs
- Regulatory Affairs Jobs
- Healthcare Compliance Careers
Working with Vantive provides valuable exposure to international medical device regulations and quality systems while contributing to patient safety across global healthcare markets.
How to Apply

