{"id":9254,"date":"2026-10-19T02:28:17","date_gmt":"2026-10-19T02:28:17","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=novumgen-regulatory-affairs-executive-recruitment"},"modified":"2026-10-19T02:28:17","modified_gmt":"2026-10-19T02:28:17","slug":"novumgen-regulatory-affairs-executive-recruitment","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=novumgen-regulatory-affairs-executive-recruitment","title":{"rendered":"Novumgen Regulatory Affairs Executive Recruitment"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p data-pm-slice=\"1 3 []\">Novumgen is inviting applications for the position of Regulatory Affairs Executive \u2013 Mexico Market at its Vadodara, Gujarat location.<br \/>The opportunity is suitable for candidates with 1\u20134 years of experience in pharmaceutical regulatory affairs.<br \/>The role involves regulatory submissions to COFEPRIS, dossier preparation, product registrations, renewals, and regulatory lifecycle management.<br \/>Interested candidates with relevant regulatory affairs experience can send their updated CV to the recruitment email address provided below.<\/p>\n<h2>Company Overview<\/h2>\n<p>Novumgen is hiring a Regulatory Affairs Executive to support pharmaceutical regulatory activities for the Mexico market. The position involves coordinating regulatory submissions, maintaining product registration documentation, and working with cross-functional teams and external partners.<\/p>\n<h2>Novumgen Regulatory Affairs Executive Job Details<\/h2>\n<h3>Position Information<\/h3>\n<ul data-spread=\"false\">\n<li><strong>Department:<\/strong> Regulatory Affairs<\/li>\n<li><strong>Designation:<\/strong> Regulatory Affairs Executive \u2013 Mexico Market<\/li>\n<li><strong>Location:<\/strong> Vadodara, Gujarat<\/li>\n<li><strong>Experience:<\/strong> 1\u20134 years<\/li>\n<\/ul>\n<h2>Job Role &amp; Responsibilities<\/h2>\n<h3>Key Responsibilities<\/h3>\n<ul data-spread=\"false\">\n<li>Prepare and coordinate regulatory submissions for pharmaceutical products to COFEPRIS, Mexico\u2019s regulatory authority.<\/li>\n<li>Support dossier preparation for new product registrations, renewals, variations, and modifications.<\/li>\n<li>Provide regulatory support to cross-functional teams.<\/li>\n<li>Handle deficiency responses for Marketing Authorization Applications.<\/li>\n<li>Coordinate with partners to ensure the timely availability of required information.<\/li>\n<li>Ensure timely submission of variations and commercial urgency requests to regulatory authorities.<\/li>\n<li>Maintain regulatory project trackers and documentation.<\/li>\n<li>Manage renewals and other regulatory lifecycle activities.<\/li>\n<\/ul>\n<h2>Eligibility &amp; Qualifications<\/h2>\n<h3>Educational Qualifications<\/h3>\n<p>Candidates should have relevant qualifications for pharmaceutical regulatory affairs. The recruitment announcement does not specify a particular degree.<\/p>\n<h3>Experience Requirements<\/h3>\n<ul data-spread=\"false\">\n<li>1\u20134 years of experience in pharmaceutical regulatory affairs.<\/li>\n<li>Familiarity with regulatory submissions and dossier preparation is relevant to the role.<\/li>\n<li>Experience with product registrations, renewals, variations, and regulatory documentation is beneficial.<\/li>\n<\/ul>\n<h3>Required Skills<\/h3>\n<ul data-spread=\"false\">\n<li>Regulatory submission coordination.<\/li>\n<li>Pharmaceutical dossier preparation and maintenance.<\/li>\n<li>Knowledge of Marketing Authorization Applications and deficiency responses.<\/li>\n<li>Regulatory project tracking and documentation management.<\/li>\n<li>Coordination with cross-functional teams and external partners.<\/li>\n<li>Ability to manage submission timelines and regulatory lifecycle activities.<\/li>\n<\/ul>\n<h2>Location &amp; Salary<\/h2>\n<h3>Job Location<\/h3>\n<p>Vadodara, Gujarat, India.<\/p>\n<h3>Salary Details<\/h3>\n<p>The salary package has not been specified in the recruitment announcement. Compensation may depend on the candidate\u2019s qualifications, experience, and the company\u2019s policies.<\/p>\n<h2>How to Apply<\/h2>\n<p>Interested candidates can share their updated CV through the recruitment email address below.<\/p>\n<p><strong>Email:<\/strong> <a rel=\"nofollow\" target=\"_blank\" href=\"http:\/\/pharmastuff.org\/cdn-cgi\/l\/email-protection#d8acb1abb0b9f6acb0b9b3b3b9aa98b6b7aeadb5bfbdb6f6bbb7b5\"><span class=\"__cf_email__\" data-cfemail=\"47332e342f2669332f262c2c263507292831322a2022296924282a\">[email\u00a0protected]<\/span><\/a><\/p>\n<h3>Application Instructions<\/h3>\n<ol start=\"1\" data-spread=\"false\">\n<li>Prepare an updated CV highlighting relevant pharmaceutical regulatory affairs experience.<\/li>\n<li>Include experience in regulatory submissions, dossier preparation, product registrations, renewals, and variations, where applicable.<\/li>\n<li>Send your CV to <a rel=\"nofollow\" target=\"_blank\" href=\"http:\/\/pharmastuff.org\/cdn-cgi\/l\/email-protection#22564b514a430c564a4349494350624c4d54574f45474c0c414d4f\"><span class=\"__cf_email__\" data-cfemail=\"95e1fce6fdf4bbe1fdf4fefef4e7d5fbfae3e0f8f2f0fbbbf6faf8\">[email\u00a0protected]<\/span><\/a>.<\/li>\n<\/ol>\n<h2>Frequently Asked Questions<\/h2>\n<h3>1. Which company is hiring for the Regulatory Affairs Executive position?<\/h3>\n<p>Novumgen is recruiting for the Regulatory Affairs Executive \u2013 Mexico Market position.<\/p>\n<h3>2. What is the required experience?<\/h3>\n<p>Candidates should have 1\u20134 years of experience.<\/p>\n<h3>3. Where is the job located?<\/h3>\n<p>The position is based in Vadodara, Gujarat.<\/p>\n<h3>4. What are the main responsibilities?<\/h3>\n<p>The role includes COFEPRIS submissions, dossier preparation, registration renewals, variations, deficiency responses, and regulatory documentation management.<\/p>\n<h3>5. How can candidates apply?<\/h3>\n<p>Candidates can email their updated CV to <a rel=\"nofollow\" target=\"_blank\" href=\"http:\/\/pharmastuff.org\/cdn-cgi\/l\/email-protection#0f7b667c676e217b676e64646e7d4f6160797a62686a61216c6062\"><span class=\"__cf_email__\" data-cfemail=\"46322f352e2768322e272d2d273406282930332b2123286825292b\">[email\u00a0protected]<\/span><\/a>.<\/p>\n<h3>6. Is a specific educational qualification mentioned?<\/h3>\n<p>The recruitment announcement does not specify a particular degree. Candidates should have relevant qualifications and experience for the role.<\/p>\n<h2>Job Summary<\/h2>\n<table>\n<tbody>\n<tr>\n<th>Category<\/th>\n<th>Details<\/th>\n<\/tr>\n<tr>\n<td>Company<\/td>\n<td>Novumgen<\/td>\n<\/tr>\n<tr>\n<td>Vacancies<\/td>\n<td>Regulatory Affairs Executive \u2013 Mexico Market<\/td>\n<\/tr>\n<tr>\n<td>Required Education<\/td>\n<td>Relevant qualification for pharmaceutical regulatory affairs<\/td>\n<\/tr>\n<tr>\n<td>Experience<\/td>\n<td>1\u20134 years<\/td>\n<\/tr>\n<tr>\n<td>Location<\/td>\n<td>Vadodara, Gujarat<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><!-- CONTENT END 1 -->\n\t\t\t<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmastuff.org\/job\/novumgen-regulatory-affairs-executive-recruitment\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":9255,"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-9254","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\/9254","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\/9255"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9254"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=9254"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=9254"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=9254"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=9254"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}