Process Validation Engineer I - Fargo, United States - Danaher Corporation

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    Description

    At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and services with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of the 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development, and delivery of solutions that safeguard and improve human health.

    The Process Validation Engineer I is part of the Technical Operations Department located in Fargo, ND, and will be an on-site role.

    At Aldevron, we combine best-in-class products and services with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Process Validation Team and report to the Supervisor of Process Validation and responsible for supporting internal and external Process Validation and Robustness activities with projects focused on standardization of documentation & processes and collaborating with key clients.

    In this role, you will have the opportunity to:

    • Evaluate and generate process flow diagrams based on key process steps, material inputs, system/equipment, process parameters, and key outputs utilizing reference documentation and stakeholder input.
    • Generate validation/verification protocols and other project-related documents that may be used to execute validation activities, and establish/improve processes utilizing reference documentation, process analysis, and cross-functional collaboration.
    • Execute and support execution of validation activities: perform operational steps of validation protocols, support and consult with other validation execution personnel, and conduct activities utilizing GMP practices with utmost integrity.
    The essential requirements of the job include:
    • B.A. or B.S. in Biology, Biochemistry, Engineering, or related science field.
    • Critical thinking and problem-solving abilities
    • Proven experience with the scientific method: experimental design, hypothesis testing, metrics, etc.

      It would be a plus if you also possess previous experience in
    • Regulated industry
    • A biotech pharmaceutical field
    At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit

    Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

    The EEO posters are available here ) .

    We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.