{"schemaVersion":"jobsearcher.job.v1","id":"b35ee1c4994cf6d32fe5dac6","url":"https://jobsearcher.com/jobs/b35ee1c4994cf6d32fe5dac6","canonicalUrl":"https://jobsearcher.com/jobs/b35ee1c4994cf6d32fe5dac6","title":"Validation Engineer","description":"*Summary:*\n\nA great opportunity for a Validation Engineer II to support QC laboratory equipment qualification activities within a world-class biopharmaceutical environment. This role ensures full compliance with cGMP, corporate quality standards, and regulatory expectations, all while contributing directly to patient safety and operational excellence.\n\n*Key Responsibilities:*\n\n* Perform equipment qualification per EQ policies and procedures\n* Partner with QC lab staff to define qualification requirements\n* Author, review & execute qualification protocols\n* Coordinate with vendors and cross-functional support teams\n* Identify quality, compliance, and operational gaps\n* Review/sign-controlled documentation per Genentech guidelines\n* Support QC operations with additional assignments\n\n*Requirements:*\n\n* BS/BA in a relevant scientific discipline (preferred).\n* Pharma or biopharma experience required.\n* Knowledge of cGMP regulations.\n* 2+ years in validation or equipment qualification (preferred).\n* Ability to manage schedules, shifting priorities, and deadlines.\n\n*Skills:*\n\n* Strong verbal & written communication.\n* Ability to influence and build relationships.\n* Strategic and execution-focused mindset.\n* High accountability and ownership of deliverables.\n\n*Environment:*\n\n* Standard office/lab setting with required safety protocols.\n\nJob Type: Contract\n\nPay: Up to $35.00 per hour\n\nExpected hours: 40 per week\n\nWork Location: In person","company":"Katalysthls","rawCompany":"katalysthls","city":"Vacaville","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-09-04T09:14:59.425Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"*Summary:*\n\nA great opportunity for a Validation Engineer II to support QC laboratory equipment qualification activities within a world-class biopharmaceutical environment. This role ensures full compliance with cGMP, corporate quality standards, and regulatory expectations, all while contributing directly to patient safety and operational excellence.\n\n*Key Responsibilities:*\n\n* Perform equipment qualification per EQ policies and procedures\n* Partner with QC lab staff to define qualification requirements\n* Author, review & execute qualification protocols\n* Coordinate with vendors and cross-functional support teams\n* Identify quality, compliance, and operational gaps\n* Review/sign-controlled documentation per Genentech guidelines\n* Support QC operations with additional assignments\n\n*Requirements:*\n\n* BS/BA in a relevant scientific discipline (preferred).\n* Pharma or biopharma experience required.\n* Knowledge of cGMP regulations.\n* 2+ years in validation or equipment qualification (preferred).\n* Ability to manage schedules, shifting priorities, and deadlines.\n\n*Skills:*\n\n* Strong verbal & written communication.\n* Ability to influence and build relationships.\n* Strategic and execution-focused mindset.\n* High accountability and ownership of deliverables.\n\n*Environment:*\n\n* Standard office/lab setting with required safety protocols.\n\nJob Type: Contract\n\nPay: Up to $35.00 per hour\n\nExpected hours: 40 per week\n\nWork Location: In person","datePosted":"2026-09-04T09:14:59.425Z","dateModified":"2026-09-04T09:14:59.425Z","hiringOrganization":{"@type":"Organization","name":"Katalysthls","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Vacaville","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b35ee1c4994cf6d32fe5dac6"},"url":"https://jobsearcher.com/jobs/b35ee1c4994cf6d32fe5dac6"}}