{"schemaVersion":"jobsearcher.job.v1","id":"1db081eeeb3b4063e545cc82","url":"https://jobsearcher.com/jobs/1db081eeeb3b4063e545cc82","canonicalUrl":"https://jobsearcher.com/jobs/1db081eeeb3b4063e545cc82","title":"Validation Engineer","description":"Position Title: Validation EngineerWork Location: Tucson, AZ 85755Assignment Duration: 12 MonthsWork Schedule: 40 hours/weekWork Arrangement: OnsitePosition Summary:* We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity.* This is an on-site position that focuses on process validation.Key Responsibilities:* Develop, write, review, and execute process validation/process verification protocols and reports.* Conduct risk assessments and develop validation strategies for new and existing processes.* Analyze and interpret process validation data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.* Collaborate with Manufacturing, Quality, Design Transfer Operations, and other departments to resolve validation issues and implement corrective actions.* Participate in process optimization and continuous improvement initiatives to enhance quality and efficiency.* Ensure compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.* Provide training and guidance to manufacturing and quality personnel on validation processes and procedures.* Maintain process validation documentation and ensure traceability and accessibility for audits and inspections.* Other duties as assigned by management.Qualification & Experience:* Bachelor's Degree in Engineering or Life Science.* Strong technical writing, analytical, and problem-solving skills.* Knowledge of cGMP and regulatory standards.* Strong understanding of process validation principles, techniques, and industry standards.","company":"Spectraforce Technologies","rawCompany":"spectraforce technologies","city":"Tucson","state":"AZ","isRemote":false,"isActive":false,"createdAt":"2026-06-02T00:36:59.147Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-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":"Position Title: Validation EngineerWork Location: Tucson, AZ 85755Assignment Duration: 12 MonthsWork Schedule: 40 hours/weekWork Arrangement: OnsitePosition Summary:* We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity.* This is an on-site position that focuses on process validation.Key Responsibilities:* Develop, write, review, and execute process validation/process verification protocols and reports.* Conduct risk assessments and develop validation strategies for new and existing processes.* Analyze and interpret process validation data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.* Collaborate with Manufacturing, Quality, Design Transfer Operations, and other departments to resolve validation issues and implement corrective actions.* Participate 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