{"id":9250,"date":"2026-10-18T16:42:45","date_gmt":"2026-10-18T16:42:45","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=vantive-wanted-executive-post-market-surveillance-pharmacovigilance"},"modified":"2026-10-18T16:42:45","modified_gmt":"2026-10-18T16:42:45","slug":"vantive-wanted-executive-post-market-surveillance-pharmacovigilance","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=vantive-wanted-executive-post-market-surveillance-pharmacovigilance","title":{"rendered":"Vantive Wanted Executive Post Market Surveillance (Pharmacovigilance)"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<h2>Vantive Recruitment \u2013 Executive, Post Market Surveillance<\/h2>\n<p>Vantive is inviting applications for the Executive \u2013 Post Market Surveillance position in Gurgaon, Haryana. This opportunity falls under the Quality Product Surveillance category and focuses on medical device complaint handling, regulatory reporting, and post-market product monitoring. The role involves reviewing customer complaints, assessing reportability, preparing Medical Device Reports (MDRs), coordinating investigations, and ensuring timely complaint closure. Candidates interested in quality assurance, medical device safety, complaint management, and regulatory compliance can review the official job listing for eligibility details.<\/p>\n<h2>Company Overview<\/h2>\n<p>Vantive is a vital organ therapy company focused on extending lives and expanding possibilities for patients and healthcare teams. With a 70-year legacy in kidney care, the company is advancing dialysis services through digital solutions and advanced therapies while investing in the development of vital organ treatments.<\/p>\n<h2>Job Details<\/h2>\n<div>\n<table>\n<tbody>\n<tr>\n<th>Particulars<\/th>\n<th>Details<\/th>\n<\/tr>\n<tr>\n<td>Company<\/td>\n<td>Vantive<\/td>\n<\/tr>\n<tr>\n<td>Job Title<\/td>\n<td>Executive \u2013 Post Market Surveillance<\/td>\n<\/tr>\n<tr>\n<td>Job ID<\/td>\n<td>JR-197514<\/td>\n<\/tr>\n<tr>\n<td>Department<\/td>\n<td>Quality Product Surveillance<\/td>\n<\/tr>\n<tr>\n<td>Job Location<\/td>\n<td>Gurgaon, Haryana, India<\/td>\n<\/tr>\n<tr>\n<td>Date Posted<\/td>\n<td>13 October 2026<\/td>\n<\/tr>\n<tr>\n<td>Job Category<\/td>\n<td>Quality Product Surveillance<\/td>\n<\/tr>\n<tr>\n<td>Official Application<\/td>\n<td><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/vantive.wd108.myworkdayjobs.com\/Vantive\/job\/Gurgaon-Haryana\/Executive--Post-Market-Surveillance_JR-197514\/apply?utm_campaign=ind%26utm_medium=jobad%26utm_content=pj_board%26utm_source=linkedin+slotted%26source=rd_van_linkedin_pj&amp;utm_source=chatgpt.com\" rel=\"nofollow noopener\" target=\"_blank\">Apply Online<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<h2>Job Role &amp; Responsibilities<\/h2>\n<p>The Executive \u2013 Post Market Surveillance will manage and process product complaints and Medical Device Reports across multiple product lines, following applicable procedures and regulatory requirements.<\/p>\n<p>Key responsibilities include:<\/p>\n<ul>\n<li>\n<div>\n<div>\n<p>Open complaint records and collect the information required for complaint processing.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Conduct written and verbal follow-ups with customers to obtain additional complaint details.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Determine whether complaints meet regulatory reporting requirements.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Prepare associated regulatory reports, including Medical Device Reports (MDRs), in accordance with applicable regulations.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Evaluate complaints to determine whether an investigation is required.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Coordinate the retrieval of product samples when necessary for investigations.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Respond to customer complaints through written and verbal communication.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Ensure timely closure of complaints in accordance with established procedures.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Manage complaint-related workflows and identify issues requiring escalation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Triage internal and external communications related to product complaints.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Participate in continuous improvement initiatives and assigned projects.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h2>Eligibility &amp; Qualifications<\/h2>\n<p>Pharmacy, Biomedical <a rel=\"nofollow\" target=\"_blank\" class=\"wpil_keyword_link\" href=\"https:\/\/pharmastuff.org\/jobs\/pharmaceutical-engineering\" target=\"_blank\" rel=\"noopener\" title=\"Engineering\" data-wpil-keyword-link=\"linked\" data-wpil-monitor-id=\"2305\">Engineering<\/a>, Biotechnology, Life Sciences, and medical device quality or regulatory affairs.<\/p>\n<h2>Key Skills &amp; Competencies<\/h2>\n<p>The responsibilities described in the listing indicate the importance of the following skills:<\/p>\n<ul>\n<li>\n<div>\n<div>\n<p>Product complaint handling and documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Complaint reportability assessment.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Medical Device Reporting (MDR) and regulatory documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Customer communication and follow-up.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Complaint investigation coordination and sample retrieval.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Workflow management and issue escalation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Compliance with established procedures.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Quality improvement and cross-functional coordination.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h2>Job Location<\/h2>\n<p>The position is based in Gurgaon, Haryana, India. The listing identifies the role under Quality Product Surveillance.<\/p>\n<h2>How to Apply<\/h2>\n<p>Interested candidates can review the official job description and submit their application through Vantive\u2019s careers portal.<\/p>\n<p><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/vantive.wd108.myworkdayjobs.com\/Vantive\/job\/Gurgaon-Haryana\/Executive--Post-Market-Surveillance_JR-197514\/apply?utm_campaign=ind%26utm_medium=jobad%26utm_content=pj_board%26utm_source=linkedin+slotted%26source=rd_van_linkedin_pj&amp;utm_source=chatgpt.com\" rel=\"nofollow noopener\" target=\"_blank\">Apply for Executive \u2013 Post Market Surveillance<\/a><\/p>\n<p>Applicants should verify the educational requirements, experience criteria, and other application details on the official portal.<\/p>\n<h2>Job Summary<\/h2>\n<div>\n<table>\n<tbody>\n<tr>\n<th>Category<\/th>\n<th>Details<\/th>\n<\/tr>\n<tr>\n<td>Company<\/td>\n<td>Vantive<\/td>\n<\/tr>\n<tr>\n<td>Vacancies (position titles)<\/td>\n<td>Executive \u2013 Post Market Surveillance<\/td>\n<\/tr>\n<tr>\n<td>Required Education<\/td>\n<td>Pharmacy, Biomedical Engineering, Biotechnology, Life Sciences, and medical device quality or regulatory affairs.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p><!-- CONTENT END 1 -->\n\t\t\t<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmastuff.org\/job\/vantive-executive-post-market-surveillance\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":9251,"template":"","meta":{"_promoted":"","_job_location":"","_application":"","_company_name":"","_company_website":"","_company_tagline":"","_company_twitter":"","_company_video":"","_filled":0,"_featured":0,"_remote_position":0,"_job_salary":"","_job_salary_currency":"","_job_salary_unit":""},"job_listing_region":[],"job-categories":[172],"job-types":[2],"job_listing_tag":[],"class_list":["post-9250","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-regulatory-affair","job_listing_type-full-time","job-type-full-time"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/9250","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings"}],"about":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/types\/job_listing"}],"author":[{"embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/media\/9251"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9250"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=9250"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=9250"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=9250"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=9250"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}