{"id":9172,"date":"2026-10-13T14:02:47","date_gmt":"2026-10-13T14:02:47","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=cubit-lifesciences-hiring-for-regulatory-affairs"},"modified":"2026-10-13T14:02:47","modified_gmt":"2026-10-13T14:02:47","slug":"cubit-lifesciences-hiring-for-regulatory-affairs","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=cubit-lifesciences-hiring-for-regulatory-affairs","title":{"rendered":"Cubit Lifesciences Hiring For Regulatory Affairs"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Cubit Lifesciences LLP is hiring experienced professionals for <strong>Regulatory Affairs (RA)<\/strong> at its Ahmedabad, Gujarat location. Candidates with 3 to 8 years of experience in regulatory affairs for oral solid dosage (OSD) or injectables, particularly across emerging markets, are invited to attend the walk-in interview.<\/p>\n<h2 class=\"wp-block-heading\">Job Details<\/h2>\n<figure class=\"wp-block-table\">\n<table class=\"has-fixed-layout\">\n<tbody>\n<tr>\n<th>Particulars<\/th>\n<th>Details<\/th>\n<\/tr>\n<tr>\n<td>Company<\/td>\n<td>Cubit Lifesciences LLP<\/td>\n<\/tr>\n<tr>\n<td>Job Role<\/td>\n<td>Regulatory Affairs (RA)<\/td>\n<\/tr>\n<tr>\n<td>Experience<\/td>\n<td>3\u20138 Years<\/td>\n<\/tr>\n<tr>\n<td>Qualifications<\/td>\n<td>B.Pharma \/ M.Pharma<\/td>\n<\/tr>\n<tr>\n<td>Dosage Forms<\/td>\n<td>OSD \/ Injectables<\/td>\n<\/tr>\n<tr>\n<td>Location<\/td>\n<td>Prahlad Nagar, Ahmedabad, Gujarat<\/td>\n<\/tr>\n<tr>\n<td>Interview Type<\/td>\n<td>Walk-in Interview<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\">Position: Regulatory Affairs (RA)<\/h2>\n<p class=\"wp-block-paragraph\">The selected candidates will handle regulatory dossier preparation and review, product registration and re-registration, regulatory submissions, variations, and product lifecycle management.<\/p>\n<h2 class=\"wp-block-heading\">Job Responsibilities<\/h2>\n<ul class=\"wp-block-list\">\n<li>Plan, prepare, and review registration and re-registration dossiers in CTD, eCTD, ACTD, and country-specific formats.<\/li>\n<li>Compile and submit regulatory queries and variations.<\/li>\n<li>Review regulatory documents and product artworks.<\/li>\n<li>Review change controls and deviations.<\/li>\n<li>Conduct gap analysis and prepare regulatory strategies for new product filings.<\/li>\n<li>Maintain product lifecycle activities.<\/li>\n<li>Coordinate with internal and external stakeholders regarding submission documents and payments.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Eligibility and Qualifications<\/h2>\n<p class=\"wp-block-paragraph\">Candidates applying for the Regulatory Affairs position must meet the following requirements:<\/p>\n<ul class=\"wp-block-list\">\n<li><strong>Educational Qualification:<\/strong> B.Pharma or M.Pharma.<\/li>\n<li><strong>Experience:<\/strong> 3 to 8 years in Regulatory Affairs.<\/li>\n<li><strong>Relevant Experience:<\/strong> Regulatory Affairs experience involving oral solid dosage (OSD) forms or injectables.<\/li>\n<li><strong>Market Experience:<\/strong> Candidates who have worked in Africa, LATAM, CIS, Asia, MENA, or other emerging markets are invited to attend the walk-in interview.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Required Skills and Expertise<\/h2>\n<p class=\"wp-block-paragraph\">Candidates should have relevant experience in:<\/p>\n<ul class=\"wp-block-list\">\n<li>CTD, eCTD, ACTD, and country-specific regulatory dossiers.<\/li>\n<li>Product registration and re-registration.<\/li>\n<li>Regulatory query and variation submissions.<\/li>\n<li>Regulatory document and artwork review.<\/li>\n<li>Change control and deviation review.<\/li>\n<li>Gap analysis and regulatory strategy preparation.<\/li>\n<li>Product lifecycle management.<\/li>\n<li>Coordination with internal and external stakeholders.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Walk-in Interview and Application Details<\/h2>\n<p class=\"wp-block-paragraph\">Eligible candidates can attend the walk-in interview at Cubit Lifesciences LLP in Ahmedabad or contact the company using the details below.<\/p>\n<p class=\"wp-block-paragraph\"><strong>Company:<\/strong> Cubit Lifesciences LLP<\/p>\n<p class=\"wp-block-paragraph\"><strong>Venue:<\/strong><br \/>Cubit Lifesciences LLP<br \/>Pinnacle Business Park, 4th Floor, B-406\/407, Corporate Road, Prahlad Nagar, Ahmedabad, Gujarat \u2013 380015.<\/p>\n<p class=\"wp-block-paragraph\"><strong>Email:<\/strong> <strong><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmabharat.org\/cubit-lifesciences-hiring-for-regulatory-affairs\/mailto:tapas@cubitgroup.in\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">tapas@cubitgroup.in<\/a><\/strong><\/p>\n<figure class=\"gb-block-image gb-block-image-2dc6659c\"><img fetchpriority=\"high\" data-lazyloaded=\"1\" fetchpriority=\"high\" decoding=\"async\" width=\"800\" height=\"997\" class=\"gb-image gb-image-2dc6659c\" src=\"https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/10\/1791858962846.jpg\" alt=\"Cubit Lifesciences Hiring For Regulatory Affairs\" title=\"1791858962846\" srcset=\"https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/10\/1791858962846.jpg 800w, https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/10\/1791858962846-241x300.jpg 241w, https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/10\/1791858962846-768x957.jpg 768w\" data-sizes=\"(max-width: 800px) 100vw, 800px\"\/><\/figure>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/cubit-lifesciences-hiring-for-regulatory-affairs\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":9173,"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-9172","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\/9172","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\/9173"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9172"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=9172"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=9172"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=9172"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=9172"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}