{"id":9244,"date":"2026-10-17T02:26:31","date_gmt":"2026-10-17T02:26:31","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=rhydburg-biotech-senior-executive-regulatory-affairs-jobs"},"modified":"2026-10-17T02:26:31","modified_gmt":"2026-10-17T02:26:31","slug":"rhydburg-biotech-senior-executive-regulatory-affairs-jobs","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=rhydburg-biotech-senior-executive-regulatory-affairs-jobs","title":{"rendered":"Rhydburg Biotech Senior Executive Regulatory Affairs Jobs"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div id=\"main\">\n<nav aria-label=\"breadcrumbs\" class=\"rank-math-breadcrumb\">\n<p><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmastuff.org\/\">Home<\/a><span class=\"separator\"> \/ <\/span><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmastuff.org\/job-listings\">Jobs<\/a><span class=\"separator\"> \/ <\/span><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmastuff.org\/jobs\/pharma-jobs-by-qualification\">Education Wise<\/a><span class=\"separator\"> \/ <\/span><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmastuff.org\/jobs\/pharmacy\">Pharmacy Jobs<\/a><\/p>\n<\/nav>\n<article id=\"post-204472\" class=\"post-204472 job_listing type-job_listing status-publish has-post-thumbnail hentry job_listing_region-dehradun job_listing_region-uttarakhand job_listing_category-b-pharmacy-jobs job_listing_category-biotechnology job_listing_category-pharma-jobs-by-qualification job_listing_category-jobs-by-department-or-designation job_listing_category-m-pharmacy job_listing_category-pharmacy job_listing_category-qa-qc job_listing_category-regulatory-medical-affairs job_listing_category-regulatory-affairs-executives job_listing_type-full-time job_listing_tag-analytical-method-validation job_listing_tag-capa job_listing_tag-clinical-research job_listing_tag-documentation job_listing_tag-method-development job_listing_tag-production job_listing_tag-qualification job_listing_tag-regulatory-compliance job_listing_tag-regulatory-submissions job_listing_tag-remote job_listing_tag-validation job_listing_experience-1-3-years job_listing_experience-3-5-years default-fi job-type-full-time\">\n<div class=\"entry-content-wrap primary-entry-content\">\n\t\t\t\t\t\t<!-- .entry-header --><\/p>\n<figure class=\"entry-media entry-img bb-vw-container1\">\n\t\t\t\t\t\t<img fetchpriority=\"high\" width=\"640\" height=\"480\" src=\"https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-900x675.webp\" class=\"attachment-large size-large wp-post-image no-lazyload\" alt=\"rhydburg-biotech-senior-executive-regulatory-affairs\" decoding=\"async\" fetchpriority=\"high\" srcset=\"https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-900x675.webp 900w, https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-451x338.webp 451w, https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-225x169.webp 225w, https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-768x576.webp 768w, https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs-624x468.webp 624w, https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/rhydburg-biotech-senior-executive-regulatory-affairs.webp 1024w\" sizes=\"(max-width: 640px) 100vw, 640px\" title=\"Rhydburg Biotech Senior Executive Regulatory Affairs Jobs 1\"\/>\t\t\t\t\t<\/figure>\n<div class=\"entry-content\">\n<div class=\"single_job_listing\">\n<div class=\"job_description\">\n<h2>Rhydburg Biotech Senior Executive \u2013 Regulatory Affairs Jobs in Dehradun<\/h2>\n<p>Rhydburg Biotech Ltd. is hiring a Senior Executive \u2013 Regulatory Affairs (JB-1702) for its pharmaceutical regulatory team in Dehradun, Uttarakhand. Candidates with a B.Pharm or M.Pharm qualification and at least 3 years of experience in Quality Assurance or analytical validation roles are eligible to apply. The position involves regulatory dossier preparation, analytical method validation document review, regulatory submissions, quality documentation, and compliance with applicable regulatory guidelines. The company lists a salary range of \u20b925,000\u2013\u20b930,000 and mentions flexible working arrangements.<\/p>\n<h2>Company Overview<\/h2>\n<p>Rhydburg Biotech Ltd. manufactures, markets, and exports generic pharmaceutical products. The company focuses on research and development, regulatory capabilities, and supplying quality products through public and private drug distribution systems.<\/p>\n<h2>Job Details<\/h2>\n<ul>\n<li>\n<div>\n<div>\n<p>Company: Rhydburg Biotech Ltd.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Designation: Senior Executive \u2013 Regulatory Affairs<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<\/li>\n<li>\n<div>\n<div>\n<p>Location: Dehradun, Uttarakhand, India<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Employment Type: Full-time<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Experience: Minimum 3 years in Quality Assurance or analytical validation roles<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Salary: \u20b925,000\u2013\u20b930,000<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Date Posted: October 14, 2026<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<\/li>\n<\/ul>\n<h2>Job Role &amp; Responsibilities<\/h2>\n<h3>Regulatory Documentation &amp; Submissions<\/h3>\n<ul>\n<li>\n<div>\n<div>\n<p>Prepare, review, and maintain regulatory documents and submissions in accordance with applicable guidelines and company procedures.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Compile and coordinate regulatory dossiers, applications, renewals, variations, amendments, and other regulatory submissions.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Maintain regulatory trackers, submission records, approvals, licenses, certificates, and related documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Prepare and coordinate responses to regulatory queries, deficiencies, observations, and requests for additional information.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h3>Analytical Data &amp; Technical Document Review<\/h3>\n<ul>\n<li>\n<div>\n<div>\n<p>Review technical documents, product specifications, analytical data, stability data, and manufacturing information for regulatory compliance.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Review analytical method validation documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Assess technical information for accuracy, completeness, and compliance with applicable requirements.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h3>Quality Assurance &amp; Cross-Functional Coordination<\/h3>\n<ul>\n<li>\n<div>\n<div>\n<p>Coordinate with Quality Assurance, Research and Development, Production, and other departments to obtain regulatory information and supporting documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Review quality documents, including deviations, Corrective and Preventive Actions (CAPA), change controls, SOPs, and batch-related records, for regulatory requirements and impact.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Support regulatory audits and inspections by preparing documents and coordinating responses with QA and relevant departments.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h3>Regulatory Compliance &amp; Data Integrity<\/h3>\n<ul>\n<li>\n<div>\n<div>\n<p>Monitor updates to regulatory guidelines and assess their impact on products, processes, documentation, and quality systems.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Ensure regulatory activities are completed within required timelines.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Maintain accurate documentation, regulatory compliance, and data integrity.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h2>Eligibility &amp; Qualifications<\/h2>\n<p>Candidates should meet the following requirements:<\/p>\n<ul>\n<li>\n<div>\n<div>\n<p>Educational Qualification: B.Pharm or M.Pharm. A bachelor\u2019s or master\u2019s degree in Pharmacy is mandatory.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Experience: Minimum 3 years of experience in Quality Assurance or analytical validation roles.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Technical Skills: Hands-on experience reviewing analytical method validation documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Analytical Skills: Ability to interpret analytical data and review technical documentation.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Regulatory Knowledge: Understanding of regulatory submissions, dossier preparation, quality documentation, and compliance requirements.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Communication Skills: Good communication skills and the ability to coordinate with cross-functional departments.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<h2>Salary &amp; Work Arrangements<\/h2>\n<ul>\n<li>\n<div>\n<div>\n<p>Salary Range: \u20b925,000\u2013\u20b930,000.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Work Location: Dehradun, Uttarakhand.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Employment Type: Full-time.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Working Arrangements: The listing mentions a remote working option with defined review responsibilities and flexible working hours aligned with dossier and submission timelines.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<li>\n<div>\n<div>\n<p>Role Focus: Technical documentation and regulatory responsibilities, without laboratory or shop-floor operations, as described in the listing.<\/p>\n<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<p>Candidates should confirm the applicable remote or office arrangement with the employer before joining.<\/p>\n<p>\u00a0<\/p>\n<h2>How to Apply<\/h2>\n<p>Interested and eligible candidates can apply through the official Rhydburg Biotech recruitment portal.<\/p>\n<p>Apply Online: <a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/rplglobal.zohorecruit.com\/jobs\/Careers\/458372000015564033\/JB-1702-Senior-Executive-Regulatory-Affairs\" rel=\"nofollow noopener\" target=\"_blank\">Rhydburg Biotech Senior Executive \u2013 Regulatory Affairs<\/a><\/p>\n<p>Applicants should highlight their pharmaceutical qualifications, Quality Assurance or analytical validation experience, analytical method validation document review skills, and regulatory documentation expertise.<\/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>Rhydburg Biotech Ltd.<\/td>\n<\/tr>\n<tr>\n<td>Vacancies (position titles)<\/td>\n<td>Senior Executive \u2013 Regulatory Affairs<\/td>\n<\/tr>\n<tr>\n<td>Required Education<\/td>\n<td>B.Pharm or M.Pharm<\/td>\n<\/tr>\n<tr>\n<td>Experience<\/td>\n<td>Minimum 3 years in Quality Assurance or analytical validation roles<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p><!-- CONTENT END 1 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