{"id":86138,"date":"2025-06-19T08:59:29","date_gmt":"2025-06-19T08:59:29","guid":{"rendered":"https:\/\/www.whitehattoolbox.com\/jobs\/regulatory-affairs-specialist\/"},"modified":"2025-06-19T08:59:29","modified_gmt":"2025-06-19T08:59:29","slug":"regulatory-affairs-specialist","status":"publish","type":"post","link":"https:\/\/www.whitehattoolbox.com\/jobs\/regulatory-affairs-specialist\/","title":{"rendered":"Regulatory Affairs Specialist"},"content":{"rendered":"<p>Key Responsibilities:   Regulatory Submissions:   Prepare and submit dossiers for product approvals to regulatory authorities (CDSCO, CE, USFDA, etc.).   Manage correspondence and follow-ups with regulatory bodies.   Compliance Management: &#8230;<\/p>\n<p><center><b><a rel=\"nofollow noopener\" href=\"https:\/\/jobviewtrack.com\/en-in\/job-1a49417f48031a0246004f1111412f0103411d1a1a53795b584e44050307540022310d061b0b04541b1a10536b4d5b4c44161c6c7511471604001a081759543b191649425c4144171b6c7511471604001a081759763b191649425c4144171b6f154610525058\/b4828f40a2cb084bb960a4dde30442c7.html?affid=0852fd5db5a52cbcd75bf945aa534932\" class=\"button purchase\" target=\"_blank\">Apply Now<\/a> <\/b><\/center><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Key Responsibilities: Regulatory Submissions: Prepare and submit dossiers for product approvals to regulatory authorities (CDSCO, CE, USFDA, etc.). Manage correspondence and follow-ups with regulatory bodies. Compliance Management: &#8230;<\/p>\n","protected":false},"author":1,"featured_media":86139,"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-86138","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\/06\/86138-regulatory-affairs-specialist.png?fit=%2C&ssl=1","jetpack-related-posts":[{"id":112898,"url":"https:\/\/www.whitehattoolbox.com\/jobs\/officer-executive-ra\/","url_meta":{"origin":86138,"position":0},"title":"Officer\/Executive \u2013 RA","author":"Admin","date":"September 8, 2025","format":false,"excerpt":"Position: Officer\/Executive \u2013 RA Location:Paria - Vapi Experience:2 - 5 Years Industries:Pharma Responsibilities: Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions. 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