{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/ohio-franklin/"},"x-facet":{"type":"city","slug":"ohio-franklin","display":"Ohio - Franklin","count":1},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c1218a9a-90a"},"title":"Quality Assurance and Control","description":"<p>At Pfizer, you will contribute to the delivery of safe and effective products to patients through your role in quality assurance and control.</p>\n<p><strong>Job Overview</strong> In this role, you will author, review, and approve validation master plans, protocols, and reports to ensure compliance with company standards and regulatory requirements.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Perform various validation activities in compliance with Good Manufacturing Practices (GMP) and Validation Master Plan (VMP) requirements.</li>\n<li>Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.</li>\n<li>Manage routine Quality systems such as Supplier Quality Management, Change Control, Quality Risk Management, Documentation, and Investigations, Annual Product Review, and coordinate testing with functional groups.</li>\n<li>Maintain the Site Validation Master Plan and support validation as a Subject Matter Expert during customer and regulatory audits.</li>\n<li>Support regulatory queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BS with at least 2+ years of experience in the pharmaceutical industry.</li>\n<li>Proven expertise in Good Manufacturing Practices.</li>\n<li>Strong working knowledge of various quality systems and processes.</li>\n<li>Familiarity with information systems such as Global Document Management System, System Application &amp; Products, and Quality Tracking System.</li>\n<li>Excellent verbal and written communication skills.</li>\n<li>Ability to work independently and in a team environment.</li>\n</ul>\n<p><strong>Preferred Qualifications</strong></p>\n<ul>\n<li>Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems.</li>\n<li>Experience with quality management systems like Veeva and Kneat.</li>\n<li>Strong analytical and problem-solving skills.</li>\n<li>Strong organizational and time management skills.</li>\n<li>Ability to mentor and guide other colleagues.</li>\n<li>Experience in regulatory audits and compliance.</li>\n<li>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot.</li>\n<li>Technical writing skills.</li>\n</ul>\n<p><strong>Physical and Mental Requirements</strong></p>\n<ul>\n<li>Ability to perform mathematical calculations and complex data analysis.</li>\n<li>Sitting, lifting, standing, and bending.</li>\n</ul>\n<p><strong>Work Schedule and Travel</strong></p>\n<ul>\n<li>Minimal travel requirements (less than 5%).</li>\n<li>Position requires regular onsite attendance; 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