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Process Technology Engineer III

Thermo Fisher Scientific

Process Technology Engineer III

full-timePosted: Aug 3, 2026Updated: Sep 1, 2026USA, Missouri, Columbia

Job Description

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materialsJob DescriptionAs part of our Process Technology Team, you will contribute to defining, enabling, and executing the manufacturing process strategy across the Filtration and Separation Division network. The team ensures the network is technically capable, capacity-aligned, cost-competitive, and scalable to meet current and future customer demand.A Day in the Life:Serve as a technical authority for manufacturing process capability and network readiness.Optimize production processes, implement new technologies, and drive continuous improvement initiatives.Ensure the efficient manufacture of high-quality products while maintaining compliance with regulatory requirementsManage process improvement projects to drive cost reductions, improve efficiencies, and enhance manufacturing capabilities across our operations.Provide technical expertise for new product introductions.Develop and validate manufacturing processes.Implement automation solutions.Work with cross-functional teams including but not limited to R&D, Quality, Production, and other departments.Requirements:Minimum Education Required: Bachelor’s degree (preferred major in Engineering (Mechanical, Chemical, Industrial or related field))Experience Required: 5+ years of experience in manufacturing engineering in a regulated industry (pharmaceutical, medical device, or similar)Experience in process validation, equipment qualification, and change control managementExperience with automation systems, PLCs, and manufacturing control systemsExperience with risk assessment methodologies and root cause analysisKnowledge, Skills, AbilitiesStrong knowledge of GMP, ISO standards, and regulatory requirementsProficient in statistical analysis and continuous improvement methodologiesStrong project management skills and ability to work with cross-functional teamsDemonstrated success implementing process improvements and cost reduction initiativesExcellent analytical and problem-solving abilitiesStrong written and verbal communication skillsAbility to work effectively in a dynamic manufacturing environmentProficiency with Microsoft Office suite and relevant engineering softwareStrong attention to detail and organizational skillsDemonstrated ability to manage multiple projects simultaneouslyKnowledge of lean manufacturing principles and toolsAbility to travel up to 25% as needed

Locations

  • USA, Missouri, Columbia

Skills Required

  • manufacturing engineering in a regulated industryintermediate
  • process validationintermediate
  • automation systemsintermediate
  • risk assessment methodologiesintermediate

Required Qualifications

  • Minimum Education Required: Bachelor’s degree (preferred major in Engineering (Mechanical, Chemical, Industrial or related field)) (degree in in engineering)
  • Experience Required: 5+ years of experience in manufacturing engineering in a regulated industry (pharmaceutical, medical device, or similar) (experience, 5 years)
  • Experience in process validation, equipment qualification, and change control management (experience)
  • Experience with automation systems, PLCs, and manufacturing control systems (experience)
  • Experience with risk assessment methodologies and root cause analysis (experience)
  • Minimum Education Required: Bachelor’s degree (preferred major in Engineering (Mechanical, Chemical, Industrial or related field)) (degree in in engineering)
  • Experience Required: 5+ years of experience in manufacturing engineering in a regulated industry (pharmaceutical, medical device, or similar) (experience, 5 years)
  • Experience in process validation, equipment qualification, and change control management (experience)
  • Experience with automation systems, PLCs, and manufacturing control systems (experience)
  • Experience with risk assessment methodologies and root cause analysis (experience)

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