{"schemaVersion":"jobsearcher.job.v1","id":"75e520d79eeb4e895b58e6dd","url":"https://jobsearcher.com/jobs/75e520d79eeb4e895b58e6dd","canonicalUrl":"https://jobsearcher.com/jobs/75e520d79eeb4e895b58e6dd","title":"Validation Engineer","description":"Job Description:\nWith direct supervision, the candidate is responsible for the support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Client principles, quality policies, standards, and core values. Maintains the company's right to operate, supply to patients, and cost-effectiveness by actively participating in continuous improvement projects.\n\nTechnical Responsibilities:\n\nPerform qualification of laboratory equipment in accordance with EQ policies, plans, and procedures.\nCoordinate with laboratory personnel to define qualification requirements.\nAuthor, review, and execute equipment qualification protocols.\nCoordinate equipment qualification activities with vendors and other support groups.\nIdentify business, quality, and compliance gaps.\nSign documents for activities as authorized and described by Client policies, procedures, and job descriptions.\nPerform any other tasks as requested by Senior Management to support QC laboratory operations.\n\nRequirements:\nEducation:\n\nBS/BA degree (preferably in a relevant scientific discipline).\n\nExperience (may vary depending on site size/scope):\n\nExperience in the pharmaceutical/biopharmaceutical industry, or an equivalent combination of education and experience.\nKnowledge of cGMP or equivalent regulations.\nMinimum of two years' experience in Validation or equipment qualification is desired.\nAbility to make sound decisions about scheduling and managing priorities.\nFlexibility in problem-solving, providing direction, and work hours to meet business objectives.\n\nKnowledge / Skills / Competencies:\n\nPossesses strong verbal and written communication skills and the ability to influence at all levels.\nCapable of building trustful and effective relationships.\nAble to think strategically and translate strategies into actionable plans.\nTakes responsibility, drives results, and achieves expected outcomes.\n\nWork Environment / Physical Demands / Safety Considerations:\n\nStandard office environment.","company":"Katalysthealthcares","rawCompany":"katalysthealthcares","city":"Augusta","state":"GA","isRemote":false,"isActive":false,"createdAt":"2026-09-02T11:12:55.696Z","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":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Job Description:\nWith direct supervision, the candidate is responsible for the support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Client principles, quality policies, standards, and core values. Maintains the company's right to operate, supply to patients, and cost-effectiveness by actively participating in continuous improvement projects.\n\nTechnical Responsibilities:\n\nPerform qualification of laboratory equipment in accordance with EQ policies, plans, and procedures.\nCoordinate with laboratory personnel to define qualification requirements.\nAuthor, review, and execute equipment qualification protocols.\nCoordinate equipment qualification activities with vendors and other support groups.\nIdentify business, quality, and compliance gaps.\nSign documents for activities as authorized and described by Client policies, procedures, and job descriptions.\nPerform any other tasks as requested by Senior Management to support QC laboratory operations.\n\nRequirements:\nEducation:\n\nBS/BA degree (preferably in a relevant scientific discipline).\n\nExperience (may vary depending on site size/scope):\n\nExperience in the pharmaceutical/biopharmaceutical industry, or an equivalent combination of education and experience.\nKnowledge of cGMP or equivalent regulations.\nMinimum of two years' experience in Validation or equipment qualification is desired.\nAbility to make sound decisions about scheduling and managing priorities.\nFlexibility in problem-solving, providing direction, and work hours to meet business objectives.\n\nKnowledge / Skills / Competencies:\n\nPossesses strong verbal and written communication skills and the ability to influence at all levels.\nCapable of building trustful and effective relationships.\nAble to think strategically and translate strategies into actionable plans.\nTakes responsibility, drives results, and achieves expected outcomes.\n\nWork Environment / Physical Demands / Safety Considerations:\n\nStandard office environment.","datePosted":"2026-09-02T11:12:55.696Z","dateModified":"2026-09-02T11:12:55.696Z","hiringOrganization":{"@type":"Organization","name":"Katalysthealthcares","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Augusta","addressRegion":"GA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"75e520d79eeb4e895b58e6dd"},"url":"https://jobsearcher.com/jobs/75e520d79eeb4e895b58e6dd"}}