{"schemaVersion":"jobsearcher.job.v1","id":"f82c8a75dce82b6d43d91292","url":"https://jobsearcher.com/jobs/f82c8a75dce82b6d43d91292","canonicalUrl":"https://jobsearcher.com/jobs/f82c8a75dce82b6d43d91292","title":"Junior Validation Engineer","description":"Company DescriptionAssure Infusions is a U.S.-based, FDA-registered 503B outsourcing facility specializing in the manufacturing of sterile, ready-to-use premixed IV bags. Our advanced, cGMP-compliant, and fully automated manufacturing platform ensures exceptional sterility, consistency, and reliability. We provide scalable IV production solutions to enhance hospital supply chains and address nationwide IV fluid shortages. Offering contract manufacturing, private-label production, and national distribution, we are committed to delivering dependable IV supplies to meet healthcare demands.Role DescriptionThis is a full-time, on-site role located in Bartow, FL, for a Junior Validation Engineer. In this role, you will be responsible for supporting the validation and qualification of equipment, systems, and processes. Key responsibilities include conducting tests and analyses, debugging issues, performing functional verification, and ensuring compliance with Good Manufacturing Practices (GMP) standards. You will work closely with cross-functional teams to document and implement validation processes that align with regulatory requirements.Key Responsibilities Validation Execution & SupportAssist with execution of validation protocols (IQ, OQ, PQ) under supervision.Perform data collection, instrument readings, sampling, and verification activities during qualification tests.Document results clearly, accurately, and contemporaneously following GDP and data integrity expectations.Documentation & CompliancePrepare draft validation documents (protocols, reports, logs, checklists) for review.Maintain controlled records, binders, and validation files in alignment with cGMP and company SOPs.Support deviations, change controls, and CAPAs related to validation activities by gathering data and assisting with documentation.Equipment & System SupportAssist with equipment startup, shutdown, calibration coordination, and test set‑ups.Support validation activities related to manufacturing equipment, utilities, cleanrooms, and computerized systems.Perform physical walkthroughs of equipment and rooms to verify configuration before and after validation testing.Cross‑Functional CollaborationWork closely with Maintenance, Quality, Production, and Laboratory teams during validation execution.Participate in project meetings as needed to assist with scheduling, protocol preparation, and data review. QualificationsBachelor's degree in Engineering or a related field Experience in Validation and Good Manufacturing Practice (GMP)Strong analytical, organizational, and problem-solving skillsAbility to collaborate in a team-oriented environment and communicate effectivelyFamiliarity with FDA guidelines and regulatory compliance is a plus","company":"Assure Infusions","rawCompany":"assure infusions","city":"Bartow","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-04-22T18:58:13.201Z","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":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Junior Validation Engineer","description":"Company DescriptionAssure Infusions is a U.S.-based, FDA-registered 503B outsourcing facility specializing in the manufacturing of sterile, ready-to-use premixed IV bags. Our advanced, cGMP-compliant, and fully automated manufacturing platform ensures exceptional sterility, consistency, and reliability. We provide scalable IV production solutions to enhance hospital supply chains and address nationwide IV fluid shortages. Offering contract manufacturing, private-label production, and national distribution, we are committed to delivering dependable IV supplies to meet healthcare demands.Role DescriptionThis is a full-time, on-site role located in Bartow, FL, for a Junior Validation Engineer. In this role, you will be responsible for supporting the validation and qualification of equipment, systems, and processes. Key responsibilities include conducting tests and analyses, debugging issues, performing functional verification, and ensuring compliance with Good Manufacturing Practices (GMP) standards. You will work closely with cross-functional teams to document and implement validation processes that align with regulatory requirements.Key Responsibilities Validation Execution & SupportAssist with execution of validation protocols (IQ, OQ, PQ) under supervision.Perform data collection, instrument readings, sampling, and verification activities during qualification tests.Document results clearly, accurately, and contemporaneously following GDP and data integrity expectations.Documentation & CompliancePrepare draft validation documents (protocols, reports, logs, checklists) for review.Maintain controlled records, binders, and validation files in alignment with cGMP and company SOPs.Support deviations, change controls, and CAPAs related to validation activities by gathering data and assisting with documentation.Equipment & System SupportAssist with equipment startup, shutdown, calibration coordination, and test set‑ups.Support validation activities related to manufacturing equipment, utilities, cleanrooms, and computerized systems.Perform physical walkthroughs of equipment and rooms to verify configuration before and after validation testing.Cross‑Functional CollaborationWork closely with Maintenance, Quality, Production, and Laboratory teams during validation execution.Participate in project meetings as needed to assist with scheduling, protocol preparation, and data review. QualificationsBachelor's degree in Engineering or a related field Experience in Validation and Good Manufacturing Practice (GMP)Strong analytical, organizational, and problem-solving skillsAbility to collaborate in a team-oriented environment and communicate effectivelyFamiliarity with FDA guidelines and regulatory compliance is a plus","datePosted":"2026-04-22T18:58:13.201Z","dateModified":"2026-04-22T18:58:13.201Z","hiringOrganization":{"@type":"Organization","name":"Assure Infusions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bartow","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"f82c8a75dce82b6d43d91292"},"url":"https://jobsearcher.com/jobs/f82c8a75dce82b6d43d91292"}}