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Executive, Post Market Surveillance

2-4 years
₹5–7 LPA
10 July 26, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Executive – Post Market Surveillance | Vantive
Location: Gurgaon, Haryana
Work Mode: On-site | Full-time
Estimated Salary: ₹5–7 LPA (based on industry benchmarks and role level)


About Vantive:
Vantive is a global leader in vital organ therapy, committed to revolutionizing kidney care and beyond through digital innovation and advanced services. With over 70 years of legacy in dialysis solutions, Vantive empowers care teams and patients to achieve longer, healthier lives.


Role Summary:
As an Executive in Post Market Surveillance, you will be responsible for evaluating product quality complaints, ensuring timely regulatory reporting, and driving continuous improvement through complaint data analysis. This role directly contributes to global product safety and compliance.


Key Responsibilities:

  • Evaluate potential product quality complaints and initiate records/actions in accordance with Quality System requirements.

  • Own and process complaint records as per internal procedures.

  • Conduct or approve reportability assessments (MDR, MIR, etc.) based on global regulations.

  • Author and submit regulatory reports to competent authorities as required.

  • Monitor complaint investigations and facilitate timely resolutions and closures.

  • Review and approve findings from cross-functional investigations (Engineering, Manufacturing, Quality, etc.).

  • Perform queries and generate complaint trend analyses to identify areas for improvement.

  • Contribute to departmental and organizational quality initiatives.


Qualifications & Skills:

  • Education: Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field.

  • Experience: 2–4 years of experience in Post Market Surveillance, Quality Assurance, or Medical Device Complaint Handling.

  • Regulatory Knowledge: Understanding of global regulatory reporting standards (e.g., MDR, MIR, FDA).

  • Technical Skills: Strong analytical and documentation skills; ability to perform data queries and generate reports.

  • Soft Skills: Excellent communication, attention to detail, and ability to work collaboratively across teams.


Why Join Vantive?

  • Be a part of a mission-driven organization focused on extending lives.

  • Join a collaborative and courageous team that values innovation and continuous improvement.

  • Opportunity to work on cutting-edge healthcare technologies and global quality systems.