• Beckman Coulter Diagnostics (Miami, FL)
    …experience, OR Doctoral degree in fieldExperience in software, test method, equipment , process , and/or design testing methodologies.Knowledge of FDA regulations, ... ISO standards, and GxP guidelines.Experience with Computer System Validation (CSV) and process validationIt would be a plus if you also possess previous… more
    JobGet (05/01/25)
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  • Integrated DNA Technologies (IDT) (Miami, FL)
    …that safeguard and improve human health.This position is part of the Operations Process Engineering Department located in Coralville, Iowa and will be on-site. At ... to populate the VAVE funnel with vetted and appropriately valued opportunitiesDevelop validation plans and assist with VAVE projects to realize efficiencies on… more
    JobGet (05/01/25)
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  • Cytiva (Miami, FL)
    …manufacturing and design, ensuring compliance with regulatory standards and driving process improvements; leading root cause analysis and CAPA initiatives, ensuring ... nonconformances to maintain product quality and customer satisfaction; overseeing manufacturing validation (IQ, OQ, PQ) and design assurance activities to support… more
    JobGet (05/01/25)
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  • Raytheon (Tucson, AZ)
    …Immigration Status Requirements: Security Clearance: DoD Clearance: Secret The Test Equipment Engineering (TEE) organization within RTX drives business success by ... Travel up to 20% to support development and/or delivery of our test environment equipment . What You Will Learn: System level test setup and operation across the… more
    JobGet (05/06/25)
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  • Beckman Coulter Diagnostics (Chaska, MN)
    …testsWork with the operations teams in support of tester installation qualification, process validation and process improvement activitiesThe essential ... maintaining a variety of off the shelf & custom equipment used to support functional testing of electro-mechanical assemblies...focused on innovative test solutions, automation, data analytics, and process improvements and want to work to build a… more
    JobGet (05/06/25)
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  • Cytiva (Miami, FL)
    …and maintain process documentation, including standard operating procedures (SOPs), process flows, and validation reports.Design, test, and implement new ... processes, managing projects, and ensuring the efficient production of high-quality medical devices and products in a regulated environment. The ideal candidate… more
    JobGet (05/01/25)
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  • Lead Validation Engineer or Specialist,…

    United Therapeutics (Silver Spring, MD)
    Validation Datalogger Software (preferably Amphenol / Ellab) + Ability to perform validation activities for equipment , process and/or computer-related ... Equipment , you'll be a subject matter expert in equipment validation , playing a key role in...enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our… more
    United Therapeutics (05/01/25)
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  • Senior Engineer, Process Validation

    Catalent Pharma Solutions (Harmans, MD)
    **Senior Engineer, Process Validation ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... Pharma Solutions in Harmans, MD is hiring a Senior Process Validation Engineer who is responsible for...who is responsible for the qualification of cGMP manufacturing equipment cleaning processes and/or manufacturing processes. It is critical… more
    Catalent Pharma Solutions (02/11/25)
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  • Process Validation Engineer II

    Danaher Corporation (Fargo, ND)
    …development and delivery of solutions that safeguard and improve human health. The Process Validation Engineer II is part of the Technical Operations Department ... discoveries worldwide. You will be a part of the Process Validation team and report to the...will have the opportunity to: + Develop and review validation documents for facilities, equipment , and processes.… more
    Danaher Corporation (04/23/25)
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  • Senior Quality Validation Specialist

    Curia (Rensselaer, NY)
    process and cleaning validation protocols and master plans, supervises validation activities such process / equipment / cleaning/ computer system ... in one or more core validation areas ( Equipment qualification, packaging, cleaning, utilities, process or...Familiar with FDA and EU regulations for pharmaceuticals and medical devices + Strong technical writing skills are required… more
    Curia (04/10/25)
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