{"id":112898,"date":"2025-09-08T05:59:54","date_gmt":"2025-09-08T05:59:54","guid":{"rendered":"https:\/\/www.whitehattoolbox.com\/jobs\/officer-executive-ra\/"},"modified":"2025-09-08T05:59:54","modified_gmt":"2025-09-08T05:59:54","slug":"officer-executive-ra","status":"publish","type":"post","link":"https:\/\/www.whitehattoolbox.com\/jobs\/officer-executive-ra\/","title":{"rendered":"Officer\/Executive \u2013 RA"},"content":{"rendered":"<p>Position: Officer\/Executive \u2013 RA<span class=\"br\"><\/span>Location:Paria &#8211; Vapi<span class=\"br\"><\/span>Experience:2 &#8211; 5 Years<span class=\"br\"><\/span>Industries:Pharma<span class=\"br\"><\/span><b>Responsibilities:<\/b><\/p>\n<ul>\n<li>Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil &#038; Mexico), African, and EU regions.<\/li>\n<li>Handle full lifecycle of product registration including new submissions, renewals.<\/li>\n<li>Review technical documentation: PDR, DMF, AMV, BMR\/BPR, Specifications, Stability Reports, BE Studies, etc.<\/li>\n<li>Address Ministry of Health (MoH) queries and manage deficiency responses.<\/li>\n<li>Manage post-approval changes and variation submissions.<\/li>\n<li>Liaise with international regulatory agents and distributors for submission coordination.<\/li>\n<li>Artwork review and approval ensuring compliance with label regulations.<\/li>\n<li>Maintain up-to-date registration database and submission tracker.<\/li>\n<li>Prepare administrative documents: POAs, LOAs, legalization support, etc.<\/li>\n<li>Conduct compliance review for change controls, tech transfer documents, and CMO<\/li>\n<li>Support site registration and GMP audits when required.<\/li>\n<li>Review and finalize Quality Agreements with partners\/clients.<\/li>\n<li>Handle pharmacovigilance documentation (via third-party support).<\/li>\n<\/ul>\n<p><b>Required Skills:<\/b><\/p>\n<ul>\n<li>Expertise in CIS, LATAM, EU, and African regulatory landscapes.<\/li>\n<li>Strong understanding of regulatory systems (e.g., ANVISA, EMA, CDSCO).<\/li>\n<li>Prior QC\/analytical lab experience (esp. with HPLC) is a plus.<\/li>\n<li>Proficient in regulatory writing and dossier compilation independently.<\/li>\n<li>Strong coordination, analytical, and document management skills<\/li>\n<\/ul>\n<p> Required Qualification: &#8211; B.Pharm\/M.Pharm<span class=\"br\"><\/span>Salary :- Upto 6.00 LPA<span class=\"br\"><\/span>If you are interested for this opening please send updated resume on same mail with following details.<span class=\"br\"><\/span>Total No. of Years Experience :-<span class=\"br\"><\/span>Current CTC :-<span class=\"br\"><\/span>Expected CTC :-<span class=\"br\"><\/span>Notice Period :-<\/p>\n<p><center><b><a rel=\"nofollow noopener\" href=\"https:\/\/www.careerjet.co.in\/jobad\/in6c2135cf0838832c351b0ace2e52681c?affid=0852fd5db5a52cbcd75bf945aa534932\" class=\"button purchase\" target=\"_blank\">Apply Now<\/a> <\/b><\/center><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Position: Officer\/Executive \u2013 RA Location:Paria &#8211; Vapi Experience:2 &#8211; 5 Years Industries:Pharma Responsibilities: Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil &amp; Mexico), African, and EU regions. Handle full lifecycle of product registration including new submissions, renewals. Review technical documentation: PDR, DMF, AMV, BMR\/BPR, Specifications, Stability Reports, BE Studies<\/p>\n","protected":false},"author":1,"featured_media":112899,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[15,26],"tags":[],"class_list":["post-112898","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-jobs-in-india","category-pharma-jobs"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"https:\/\/i0.wp.com\/www.whitehattoolbox.com\/jobs\/wp-content\/uploads\/2025\/09\/112898-officer-executive-ra.png?fit=%2C&ssl=1","jetpack-related-posts":[{"id":157299,"url":"https:\/\/www.whitehattoolbox.com\/jobs\/were-hiring-regulatory-affairs-manager-singapore\/","url_meta":{"origin":112898,"position":0},"title":"We\u2019re Hiring Regulatory Affairs Manager \u2013 Singapore","author":"Admin","date":"March 15, 2026","format":false,"excerpt":"A leading global pharmaceutical organization is seeking an experienced Regulatory Affairs Manager to lead regulatory strategy and submissions for Singapore. 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