{"id":7860,"date":"2026-08-25T19:08:44","date_gmt":"2026-08-25T19:08:44","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=bliss-gvs-pharma-hiring-for-research-development"},"modified":"2026-08-25T19:08:44","modified_gmt":"2026-08-25T19:08:44","slug":"bliss-gvs-pharma-hiring-for-research-development","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=bliss-gvs-pharma-hiring-for-research-development","title":{"rendered":"Bliss GVS Pharma Hiring For Research &#038; Development"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Bliss GVS Pharma Ltd. is hiring experienced pharmaceutical professionals for an <strong>Executive \u2013 R&amp;D Documentation<\/strong> position within its Research &amp; Development department. The opening is based at the company\u2019s <strong>Andheri R&amp;D facility in Mumbai<\/strong> and will support both <strong>Analytical Research &amp; Development (ARD)<\/strong> and <strong>Formulation Research &amp; Development (FRD)<\/strong> documentation activities.<\/p>\n<p class=\"wp-block-paragraph\">This <strong>Bliss GVS Pharma R&amp;D Documentation job<\/strong> is suitable for candidates with an <strong>M.Sc in Chemistry or M.Pharm<\/strong> and at least <strong>6 years of relevant R&amp;D documentation experience<\/strong> in a regulated pharmaceutical organization. Candidates with strong knowledge of cGMP, GDP, QMS, pharmacopoeial requirements, SAP, technology transfer documentation and regulatory compliance are encouraged to apply.<\/p>\n<h2 class=\"wp-block-heading\">Bliss GVS Pharma Job Overview<\/h2>\n<figure class=\"wp-block-table\">\n<table class=\"has-fixed-layout\">\n<tbody>\n<tr>\n<th>Particular<\/th>\n<th>Details<\/th>\n<\/tr>\n<tr>\n<td><strong>Company<\/strong><\/td>\n<td>Bliss GVS Pharma Ltd.<\/td>\n<\/tr>\n<tr>\n<td><strong>Department<\/strong><\/td>\n<td>Research &amp; Development<\/td>\n<\/tr>\n<tr>\n<td><strong>Designation<\/strong><\/td>\n<td>Executive (ARD &amp; FRD)<\/td>\n<\/tr>\n<tr>\n<td><strong>Function<\/strong><\/td>\n<td>R&amp;D Documentation<\/td>\n<\/tr>\n<tr>\n<td><strong>Qualification<\/strong><\/td>\n<td>M.Sc Chemistry \/ M.Pharm<\/td>\n<\/tr>\n<tr>\n<td><strong>Experience<\/strong><\/td>\n<td>Minimum 6 Years<\/td>\n<\/tr>\n<tr>\n<td><strong>Location<\/strong><\/td>\n<td>Andheri, Mumbai, Maharashtra<\/td>\n<\/tr>\n<tr>\n<td><strong>Industry<\/strong><\/td>\n<td>Pharmaceutical<\/td>\n<\/tr>\n<tr>\n<td><strong>Employment Type<\/strong><\/td>\n<td>Full-Time<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\">Key Responsibilities<\/h2>\n<p class=\"wp-block-paragraph\">The selected Executive \u2013 R&amp;D Documentation professional will be responsible for managing controlled documentation for the ARD and FRD functions while ensuring compliance with applicable pharmaceutical regulatory and cGMP requirements.<\/p>\n<ul class=\"wp-block-list\">\n<li>Prepare, review and update <strong>SOPs, specifications, Standard Testing Procedures (STPs), Batch Manufacturing Records (BMRs), Master Formula Records (MFRs), Product Development Reports (PDRs), protocols and reports<\/strong>.<\/li>\n<li>Prepare and implement product-specific documents including specifications, STPs, MFRs and <strong>Technology Transfer documentation<\/strong>.<\/li>\n<li>Generate, maintain and manage relevant <strong>SAP codes<\/strong> for materials and controlled documents.<\/li>\n<li>Prepare and review documentation associated with <strong>change controls, pharmacopoeial updates and Quality Management Systems (QMS)<\/strong>.<\/li>\n<li>Review documentation related to non-conformances, investigations and <strong>Corrective and Preventive Actions (CAPA)<\/strong>.<\/li>\n<li>Support preparation of responses to regulatory authority queries, observations and deficiencies.<\/li>\n<li>Coordinate the timely implementation and availability of approved controlled documents across relevant departments.<\/li>\n<li>Ensure documentation activities comply with <strong>Good Documentation Practices (GDP)<\/strong>, cGMP and applicable regulatory requirements.<\/li>\n<li>Support ARD and FRD teams in maintaining accurate, traceable and inspection-ready pharmaceutical R&amp;D documentation.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Qualification &amp; Experience<\/h2>\n<p class=\"wp-block-paragraph\">Candidates applying for the <strong>Bliss GVS Pharma Executive R&amp;D Documentation vacancy<\/strong> should meet the following requirements:<\/p>\n<p class=\"wp-block-paragraph\"><strong>Qualification:<\/strong> M.Sc in Chemistry or M.Pharm.<\/p>\n<p class=\"wp-block-paragraph\"><strong>Experience:<\/strong> Minimum <strong>6 years of R&amp;D Documentation experience<\/strong> within a regulated pharmaceutical company.<\/p>\n<p class=\"wp-block-paragraph\">Candidates should have practical exposure to pharmaceutical research and development documentation, particularly documentation supporting <strong>Analytical R&amp;D (ARD) and Formulation R&amp;D (FRD)<\/strong> operations.<\/p>\n<h2 class=\"wp-block-heading\">Skills Required<\/h2>\n<p class=\"wp-block-paragraph\">Applicants should possess strong knowledge of:<\/p>\n<ul class=\"wp-block-list\">\n<li>Indian Pharmacopoeia (IP), British Pharmacopoeia (BP), European Pharmacopoeia (EP) and United States Pharmacopeia (USP)<\/li>\n<li>Quality Management Systems (QMS)<\/li>\n<li>SOP preparation and document control<\/li>\n<li>Analytical and formulation development processes<\/li>\n<li>Current Good Manufacturing Practices (cGMP)<\/li>\n<li>Good Documentation Practices (GDP\/cGDP)<\/li>\n<li>Pharmaceutical regulatory guidelines<\/li>\n<li>Change control, investigations and CAPA documentation<\/li>\n<li>Technology Transfer documentation<\/li>\n<li>MS Word and Microsoft Excel<\/li>\n<li>SAP systems and document\/material code management<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Why Consider This Opportunity?<\/h2>\n<p class=\"wp-block-paragraph\">This role provides experienced pharmaceutical R&amp;D professionals an opportunity to work across <strong>ARD and FRD documentation activities<\/strong> in a regulated pharmaceutical environment. The position offers exposure to product documentation, technology transfer, QMS, regulatory responses, pharmacopoeial updates and cross-functional R&amp;D operations.<\/p>\n<p class=\"wp-block-paragraph\">Professionals seeking to strengthen their careers in <strong>pharmaceutical R&amp;D documentation, regulatory compliance, document control and quality systems<\/strong> may find the position particularly relevant.<\/p>\n<h2 class=\"wp-block-heading\">How to Apply for Bliss GVS Pharma R&amp;D Documentation Job<\/h2>\n<p class=\"wp-block-paragraph\">Interested and eligible candidates can send their <strong>updated CV\/resume<\/strong> to:<\/p>\n<p class=\"wp-block-paragraph\"><strong>Email:<\/strong> <strong><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmabharat.org\/bliss-gvs-pharma-hiring-for-research-development\/mailto:hr.careers@blissgvs.com\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">hr.careers@blissgvs.com<\/a><\/strong><\/p>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/bliss-gvs-pharma-hiring-for-research-development\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":7861,"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":[173],"job-types":[3],"job_listing_tag":[],"class_list":["post-7860","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-research-development","job_listing_type-part-time","job-type-part-time"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/7860","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\/7861"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=7860"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=7860"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=7860"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=7860"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=7860"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}