{"id":8140,"date":"2026-09-05T06:38:17","date_gmt":"2026-09-05T06:38:17","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=avenza-pharmaceuticals-hiring-for-quality-assurance"},"modified":"2026-09-05T06:38:17","modified_gmt":"2026-09-05T06:38:17","slug":"avenza-pharmaceuticals-hiring-for-quality-assurance","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=avenza-pharmaceuticals-hiring-for-quality-assurance","title":{"rendered":"Avenza Pharmaceuticals Hiring For Quality Assurance"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Avenza Pharmaceuticals Pvt Ltd has announced new <strong>Quality Assurance jobs in Vadodara<\/strong> for experienced pharmaceutical professionals. The company is recruiting for <strong>QA-IPQA<\/strong> and <strong>Qualification &amp; Validation<\/strong> positions at its HPRA-approved plant located at Jarod, Samlaya, Vadodara, Gujarat.<\/p>\n<p class=\"wp-block-paragraph\">This Avenza Pharmaceuticals recruitment drive offers opportunities for professionals with <strong>2 to 5 years of relevant pharmaceutical industry experience<\/strong> in IPQA, qualification, validation, documentation, deviation handling and regulatory compliance.<\/p>\n<p class=\"wp-block-paragraph\">Candidates looking for <strong>pharma QA jobs in Vadodara<\/strong>, <strong>IPQA jobs in Gujarat<\/strong>, or <strong>pharmaceutical validation jobs<\/strong> can review the eligibility and application details below.<\/p>\n<h2 class=\"wp-block-heading\">Avenza Pharmaceuticals Vacancy 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>Company<\/td>\n<td>Avenza Pharmaceuticals Pvt Ltd<\/td>\n<\/tr>\n<tr>\n<td>Department<\/td>\n<td>Quality Assurance<\/td>\n<\/tr>\n<tr>\n<td>Positions<\/td>\n<td>QA-IPQA; Qualification &amp; Validation<\/td>\n<\/tr>\n<tr>\n<td>Total Vacancies<\/td>\n<td>4<\/td>\n<\/tr>\n<tr>\n<td>QA-IPQA Vacancies<\/td>\n<td>3<\/td>\n<\/tr>\n<tr>\n<td>Qualification &amp; Validation Vacancies<\/td>\n<td>1<\/td>\n<\/tr>\n<tr>\n<td>Experience<\/td>\n<td>2\u20135 years, depending on position<\/td>\n<\/tr>\n<tr>\n<td>Location<\/td>\n<td>Jarod, Samlaya, Vadodara, Gujarat<\/td>\n<\/tr>\n<tr>\n<td>Plant Status<\/td>\n<td>HPRA Approved Plant<\/td>\n<\/tr>\n<tr>\n<td>Application Mode<\/td>\n<td>Email<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\">1. QA-IPQA \u2013 3 Vacancies<\/h2>\n<p class=\"wp-block-paragraph\"><strong>Experience Required:<\/strong> 2\u20134 years<\/p>\n<p class=\"wp-block-paragraph\">The QA-IPQA role focuses on maintaining quality and GMP compliance during pharmaceutical manufacturing operations.<\/p>\n<h3 class=\"wp-block-heading\">Key Responsibilities<\/h3>\n<ul class=\"wp-block-list\">\n<li>Perform in-process quality assurance activities.<\/li>\n<li>Conduct line clearance before manufacturing and packaging operations.<\/li>\n<li>Perform and document in-process checks.<\/li>\n<li>Maintain accurate IPQA documentation and records.<\/li>\n<li>Prepare IPQA reports.<\/li>\n<li>Support deviation identification, documentation and handling.<\/li>\n<li>Ensure manufacturing activities are performed according to approved procedures and applicable quality requirements.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">2. Qualification &amp; Validation \u2013 1 Vacancy<\/h2>\n<p class=\"wp-block-paragraph\"><strong>Experience Required:<\/strong> 4\u20135 years<\/p>\n<p class=\"wp-block-paragraph\">This Quality Assurance position focuses on pharmaceutical equipment, utilities, systems and process qualification and validation.<\/p>\n<h3 class=\"wp-block-heading\">Key Responsibilities<\/h3>\n<ul class=\"wp-block-list\">\n<li>Perform equipment and utilities qualification activities.<\/li>\n<li>Handle process qualification and validation.<\/li>\n<li>Conduct validation of equipment, systems and manufacturing processes.<\/li>\n<li>Support cleaning validation activities.<\/li>\n<li>Prepare qualification and validation protocols.<\/li>\n<li>Review and finalize validation reports and associated documentation.<\/li>\n<li>Maintain documentation in accordance with applicable regulatory requirements.<\/li>\n<li>Ensure qualification and validation activities comply with pharmaceutical quality standards.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Qualification &amp; Eligibility<\/h2>\n<p class=\"wp-block-paragraph\">The employer advertisement specifies the required experience but <strong>does not explicitly mention an educational qualification<\/strong>.<\/p>\n<p class=\"wp-block-paragraph\">Based on the nature of pharmaceutical Quality Assurance, IPQA, qualification and validation functions, candidates commonly considered for similar positions may hold:<\/p>\n<ul class=\"wp-block-list\">\n<li>B.Pharm<\/li>\n<li>M.Pharm<\/li>\n<li>B.Sc in a relevant science discipline<\/li>\n<li>M.Sc in a relevant science discipline<\/li>\n<\/ul>\n<p class=\"wp-block-paragraph\"><strong>Important:<\/strong> These degrees are editorial guidance and are <strong>not explicitly listed in the Avenza Pharmaceuticals recruitment notice<\/strong>. Candidates should confirm their educational eligibility directly with the employer before applying.<\/p>\n<p class=\"wp-block-paragraph\">For <strong>QA-IPQA<\/strong>, applicants should have approximately <strong>2\u20134 years of relevant experience<\/strong>. Candidates applying for <strong>Qualification &amp; Validation<\/strong> should have approximately <strong>4\u20135 years of relevant experience<\/strong>.<\/p>\n<h2 class=\"wp-block-heading\">Key Skills<\/h2>\n<p class=\"wp-block-paragraph\">Relevant skills for these Avenza Pharmaceuticals QA jobs include <strong>IPQA, line clearance, in-process quality checks, GMP documentation, deviation handling, equipment qualification, utility qualification, process validation, cleaning validation, validation protocols, validation reports and regulatory compliance<\/strong>.<\/p>\n<h2 class=\"wp-block-heading\">Why Consider This Opportunity?<\/h2>\n<p class=\"wp-block-paragraph\">The recruitment is for Avenza Pharmaceuticals\u2019 <strong>HPRA-approved plant<\/strong>, providing experienced QA professionals an opportunity to work in a regulated pharmaceutical manufacturing environment.<\/p>\n<p class=\"wp-block-paragraph\">The positions provide exposure to important Quality Assurance functions including shop-floor IPQA, documentation, deviation management, equipment and utility qualification, process validation and cleaning validation.<\/p>\n<p class=\"wp-block-paragraph\"><strong>Note:<\/strong> The employer advertisement does not specify salary, employee benefits, incentives or other compensation details. Candidates should discuss these directly during the recruitment process.<\/p>\n<h2 class=\"wp-block-heading\">How to Apply for Avenza Pharmaceuticals Jobs<\/h2>\n<p class=\"wp-block-paragraph\">Interested candidates should send an updated resume to:<\/p>\n<p class=\"wp-block-paragraph\"><strong>Email:<\/strong> <strong><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmabharat.org\/avenza-pharmaceuticals-hiring-for-quality-assurance\/mailto:recruitment@avenzapharma.com\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">recruitment@avenzapharma.com<\/a><\/strong><\/p>\n<figure class=\"gb-block-image gb-block-image-67cf2bc5\"><img fetchpriority=\"high\" data-lazyloaded=\"1\" fetchpriority=\"high\" decoding=\"async\" width=\"608\" height=\"903\" class=\"gb-image gb-image-67cf2bc5\" src=\"https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/09\/Screenshot-2026-09-05-104912.png\" alt=\"Avenza Pharmaceuticals Hiring For Quality Assurance\" title=\"Screenshot 2026-09-05 104912\" srcset=\"https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/09\/Screenshot-2026-09-05-104912.png 608w, https:\/\/pharmabharat.org\/wp-content\/uploads\/2026\/09\/Screenshot-2026-09-05-104912-202x300.png 202w\" data-sizes=\"(max-width: 608px) 100vw, 608px\"\/><\/figure>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/avenza-pharmaceuticals-hiring-for-quality-assurance\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":8141,"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":[171],"job-types":[],"job_listing_tag":[],"class_list":["post-8140","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-qc"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/8140","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\/8141"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=8140"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=8140"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=8140"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=8140"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=8140"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}