Vantive Hiring Executive - Post Market Surveillance
Are you seeking Vantive Careers Gurgaon or a Medical Device Vigilance Job in Haryana? Global vital organ therapies leader Vantive has announced openings for Executive, Post Market Surveillance (Job ID: JR-196010) to support its vigilance division.
This post-market compliance surveillance and medical device reporting vacancy is ideal for science, biomedical engineering, or pharmacy graduates with 1 or more years of experience documenting customer complaints, tracking device returns, and archiving regulatory files. Selected executives will perform customer follow-ups and draft MDR reports. To write a resume detailing your complaint closing speed, sample triage, or database tracking milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Vantive (Vantive Healthcare Technologies Private Limited) |
| Position | Executive, Post Market Surveillance |
| Job Requisition ID | JR-196010 |
| Job Location | Gurgaon, Haryana, India |
| Employment Type | Full-Time (Office-Based) |
| Experience Required | 1 Year+ (0–3 years experience preferred) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc in Life Sciences, Biomedical Engineering, Biotechnology |
| Expected CTC | ₹4,80,000 – ₹7,50,000 per annum (Estimated) |
💼 Key Responsibilities
- Complaint Triage: Review and open complaint files for medical devices, categorizing severity levels.
- Customer Communication: Perform verbal and written customer follow-ups to collect missing product or clinical details.
- Reportability Reviews: Assess complaint criteria under regulatory guidelines to determine if global alerts are required.
- MDR Preparation: Write and submit Medical Device Reports (MDRs) in compliance with national health authority timelines.
- Sample Retrieval: Coordinate sample returns from clinical locations for physical lab investigations.
- Timely Closures: Drive complaint files from initial triage to record closure within SOP schedules.
To learn how medical device vigilance and post-market safety executive salaries compare to conventional pharmacovigilance drug safety associate and clinical programming roles, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master’s degree in Pharmacy, Life Sciences, Biomedical Engineering, or Biotechnology.
- Core Experience: Experience in medical device complaint handling, post-market surveillance, or pharmacovigilance.
- Regulatory Knowledge: Basic understanding of Medical Device Reporting (MDR) rules and safety reporting timelines.
- Communication Skills: Excellent spoken and written English to follow up with international clinicians and customers.
- System Capabilities: Proficient in Microsoft Office (specifically Word data entry and Excel trackers).
For pharmacy graduates evaluating medical device vigilance pathways compared to conventional laboratory quality control, clinical trial administration, or chemical formulation careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Vantive?
- Work inside a specialized vital organ therapies company building on a 70-year legacy of kidney care.
- Build deep expertise in international medical device regulations, vigilance systems, and global audits.
- Access structured employee wellness initiatives and professional career development programs.
- Enjoy a professional office working environment located in the Gurgaon business zone.
To review your basic knowledge of clinical registers, patient safety protocols, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 PMS Executive vs Healthcare IT
PMS Executives document device complaints, draft regulatory reports (MDRs), and coordinate sample returns, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Vantive Candidates
- Highlight Medical Device Knowledge: If you worked with specific device lines (hemodialysis, pumps, catheters), list them.
- Specify Vigilance Standards: Mention any experience with ISO 13485, FDA 21 CFR Part 803, or EU MDR guidelines.
- Detail Case Metrics: Emphasize experience processing high case volumes, noting timelines and accuracy rates.
💬 Vantive Post Market Surveillance Interview Questions
- Q1. What is the difference between a medical device complaint and a spontaneous adverse drug event?
Answer Guidance: A device complaint focuses on any written, electronic, or oral communication that alleges deficiencies related to the identity, quality, durability, reliability, safety, effectiveness, or performance of a marketed device. An adverse drug event focuses on patient symptoms caused by drug substance exposure. - Q2. What is a Medical Device Report (MDR) and when is it required?
Answer Guidance: An MDR is a regulatory report submitted to authorities (like the FDA) when a manufacturer receives information that a device may have caused or contributed to a death or serious injury, or has malfunctioned in a way that could cause harm. - Q3. How do you prioritize cases when you receive multiple complaints in one day?
Answer Guidance: I prioritize based on severity and reporting timelines, indexing cases involving patient injury or death first, followed by malfunctions with high occurrence rates, and finally low-risk administrative records.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Vantive's official Workday careers board. Click the button below to apply:
Apply Online – Vantive Workday Board❓ Frequently Asked Questions
Q. Do I need a B.Pharm degree to apply for this Vantive position?
While B.Pharm/M.Pharm is accepted, Vantive also welcomes graduates holding degrees in Life Sciences, Biomedical Engineering, or Biotechnology.
Q. Is this post-market surveillance role remote?
No, this is a full-time, office-based role located at Vantive's office in Gurgaon, Haryana, India.
Q. What is the required experience level?
Vantive prefers candidates with 0 to 3 years of experience (1 year+ relevant experience is highly preferred).
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