{"schemaVersion":"jobsearcher.job.v1","id":"e8459501c3bdc51edff56a59","url":"https://jobsearcher.com/jobs/e8459501c3bdc51edff56a59","canonicalUrl":"https://jobsearcher.com/jobs/e8459501c3bdc51edff56a59","title":"Validation Engineer","description":"Overview\nIn this role you support and execute QC equipment qualification under cGMP, collaborating with lab teams and vendors to ensure compliant, efficient operations. You contribute to continuous improvement projects that sustain quality and operational readiness. You will work under supervision to maintain the company’s right to operate and supply patients. This is a hands-on role with a clear impact on quality and compliance.\n\nCompensation / Benefitscompetitive pay ($45-$50/hr)\nResponsibilitiesQualify laboratory equipment in line with EQ policies, plans, and proceduresCoordinate with laboratory personnel to determine qualification needsAuthor, review, and execute equipment qualification protocolsCoordinate qualification activities with vendors and support groupsIdentify business, quality, and compliance gapsSign documents as authorized by policies and job descriptionsSupport QC operations with additional tasks as needed by Senior Management\nKey requirementsBS/BA in a relevant scientific disciplineExperience in pharmaceutical/biopharmaceutical industry or equivalentKnowledge of cGMP or equivalent regulationsMinimum of two years in Validation or equipment qualification (preferred)Ability to manage priorities and schedulingFlexibility in problem-solving and work hoursStrong verbal and written communicationAbility to build trustful relationshipsStrategic thinking and translation of strategies into actionable plansEquipment qualification and validationProtocol authoring and reviewVendor and cross-group coordination","company":"Planet Pharma","rawCompany":"planet pharma","city":"Fairfield","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-09-15T03:45:37.784Z","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":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Overview\nIn this role you support and execute QC equipment qualification under cGMP, collaborating with lab teams and vendors to ensure compliant, efficient operations. You contribute to continuous improvement projects that sustain quality and operational readiness. You will work under supervision to maintain the company’s right to operate and supply patients. This is a hands-on role with a clear impact on quality and compliance.\n\nCompensation / Benefitscompetitive pay ($45-$50/hr)\nResponsibilitiesQualify laboratory equipment in line with EQ policies, plans, and proceduresCoordinate with laboratory personnel to determine qualification needsAuthor, review, and execute equipment qualification protocolsCoordinate qualification activities with vendors and support groupsIdentify business, quality, and compliance gapsSign documents as authorized by policies and job descriptionsSupport QC operations with additional tasks as needed by Senior Management\nKey requirementsBS/BA in a relevant scientific disciplineExperience in pharmaceutical/biopharmaceutical industry or equivalentKnowledge of cGMP or equivalent regulationsMinimum of two years in Validation or equipment qualification (preferred)Ability to manage priorities and schedulingFlexibility in problem-solving and work hoursStrong verbal and written communicationAbility to build trustful relationshipsStrategic thinking and translation of strategies into actionable plansEquipment qualification and validationProtocol authoring and reviewVendor and cross-group coordination","datePosted":"2026-09-15T03:45:37.784Z","dateModified":"2026-09-15T03:45:37.784Z","hiringOrganization":{"@type":"Organization","name":"Planet Pharma","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Fairfield","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e8459501c3bdc51edff56a59"},"url":"https://jobsearcher.com/jobs/e8459501c3bdc51edff56a59"}}