{"id":9042,"date":"2026-10-08T11:51:24","date_gmt":"2026-10-08T11:51:24","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=credevo-hiring-for-quality-assurance-associate"},"modified":"2026-10-08T11:51:24","modified_gmt":"2026-10-08T11:51:24","slug":"credevo-hiring-for-quality-assurance-associate","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=credevo-hiring-for-quality-assurance-associate","title":{"rendered":"Credevo Hiring For Quality Assurance Associate"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Credevo is hiring for the position of <strong>Quality Assurance Associate<\/strong> on a <strong>remote<\/strong> basis. The role requires <strong>4+ years of experience<\/strong> and an <strong>immediate joiner<\/strong>. The position focuses on quality assurance, GCP compliance, clinical trial data integrity, documentation, audits, and process improvement.<\/p>\n<h2 class=\"wp-block-heading\">Job Details<\/h2>\n<figure class=\"wp-block-table\">\n<table class=\"has-fixed-layout\">\n<tbody>\n<tr>\n<th>Job Details<\/th>\n<th>Information<\/th>\n<\/tr>\n<tr>\n<td><strong>Company<\/strong><\/td>\n<td>Credevo<\/td>\n<\/tr>\n<tr>\n<td><strong>Job Title<\/strong><\/td>\n<td>Quality Assurance Associate<\/td>\n<\/tr>\n<tr>\n<td><strong>Experience<\/strong><\/td>\n<td>4+ years<\/td>\n<\/tr>\n<tr>\n<td><strong>Job Location<\/strong><\/td>\n<td>Remote<\/td>\n<\/tr>\n<tr>\n<td><strong>Joining<\/strong><\/td>\n<td>Immediate Joiner<\/td>\n<\/tr>\n<tr>\n<td><strong>Education<\/strong><\/td>\n<td>Bachelor\u2019s degree in a related field<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\">Position<\/h2>\n<h3 class=\"wp-block-heading\">Quality Assurance Associate<\/h3>\n<p class=\"wp-block-paragraph\">The Quality Assurance Associate will support QA processes in clinical research, ensuring compliance with <strong>Good Clinical Practice (GCP), SOPs, regulatory requirements, and company policies<\/strong>. The role also involves clinical trial data review, audits, documentation, risk management, and process improvement.<\/p>\n<h2 class=\"wp-block-heading\">Key Responsibilities<\/h2>\n<h3 class=\"wp-block-heading\">Data Integrity and Accuracy<\/h3>\n<ul class=\"wp-block-list\">\n<li>Review and verify clinical trial data for accuracy, completeness, and consistency.<\/li>\n<li>Ensure clinical trial data is generated, recorded, and reported according to protocols, SOPs, and GCP.<\/li>\n<li>Participate in data validation and reconciliation activities.<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\">Compliance and Regulatory Adherence<\/h3>\n<ul class=\"wp-block-list\">\n<li>Maintain knowledge of GCP guidelines, regulatory requirements, and company policies.<\/li>\n<li>Ensure clinical trial activities comply with relevant regulations and guidelines.<\/li>\n<li>Assist with preparation for and participation in audits and inspections.<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\">Documentation and Record Keeping<\/h3>\n<ul class=\"wp-block-list\">\n<li>Maintain accurate and complete documentation of QA activities.<\/li>\n<li>Ensure proper storage and retrieval of clinical trial documents.<\/li>\n<li>Assist in developing and maintaining SOPs.<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\">Process Improvement<\/h3>\n<ul class=\"wp-block-list\">\n<li>Identify areas for improvement in clinical trial processes and procedures.<\/li>\n<li>Contribute to the development and implementation of quality assurance plans.<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\">Collaboration and Communication<\/h3>\n<ul class=\"wp-block-list\">\n<li>Collaborate with clinical research associates, data managers, and regulatory affairs staff.<\/li>\n<li>Communicate findings and recommendations to management and stakeholders.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Eligibility and Qualifications<\/h2>\n<p class=\"wp-block-paragraph\">Candidates should have:<\/p>\n<ul class=\"wp-block-list\">\n<li><strong>4+ years of experience<\/strong><\/li>\n<li>A <strong>Bachelor\u2019s degree in a related field<\/strong>, such as:\n<ul class=\"wp-block-list\">\n<li>Life Sciences<\/li>\n<li>Pharmacy<\/li>\n<li>Nursing<\/li>\n<\/ul>\n<\/li>\n<li>Familiarity with <strong>GCP guidelines and regulatory requirements<\/strong><\/li>\n<li>Knowledge of <strong>clinical trial data management systems and electronic data capture (EDC) systems<\/strong><\/li>\n<li>Understanding of clinical trial processes and procedures<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Required Skills<\/h2>\n<ul class=\"wp-block-list\">\n<li>Strong attention to detail and accuracy<\/li>\n<li>Excellent organizational and communication skills<\/li>\n<li>Ability to work independently and as part of a team<\/li>\n<li>Proficiency in data analysis and interpretation<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Application Details<\/h2>\n<p class=\"wp-block-paragraph\">Interested candidates can apply for the <strong>Quality Assurance Associate<\/strong> position through the application form provided below.<\/p>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/credevo-hiring-for-quality-assurance-associate\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":9043,"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":[170],"job-types":[],"job_listing_tag":[],"class_list":["post-9042","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-qa"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/9042","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\/9043"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9042"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=9042"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=9042"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=9042"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=9042"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}