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LM
Leica Microsystems Inc
Process Validation Engineering Co-Op
Entry-Level JobVerifiedNo experience needed
Career Insights for Validation Engineer
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Based on North Dakota data
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What they do
A Validation Engineer evaluates and maintains machinery and equipment used in manufacturing, and supervises workers that use and repair the machines.
$99,941 / year median in North Dakota
+5% projected growth
Job Description
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers . As a member of our team, you'll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time. Learn about the Danaher Business System which makes everything possible. The Process Validation Engineering Co-op is responsible for supporting process validation activities across the biologics manufacturing lifecycle, including process design, process qualification, and continued process verification. This position reports to the Manager, Process Validation and is part of the Technical Operations team located in Fargo, North Dakota and will be an on-site role. In this role, you will have the opportunity to: Support the development, execution, and reporting of process validation activities for biologics manufacturing processes. Participate in ancillary validation studies including aseptic process simulations (APS/media fills), equipment performance qualifications (PQ), cleaning validation studies, hold-time studies, container closure integrity testing (CCIT), and other GMP qualification and validation activities. Collaborate with cross-functional teams including Manufacturing, Manufacturing Science and Technology (MSAT), Quality Assurance, Quality Control, Engineering, and Regulatory Affairs to execute validation deliverables. The essential requirements of the job include: Currently pursuing a Bachelor's degree in Chemical Engineering, Bioprocess Engineering, Biomedical Engineering, Biological Systems Engineering, Biotechnology, or a related STEM discipline. Ability to interpret technical data and apply scientific principles to engineering and manufacturing challenges within a regulated environment. Proficiency with Microsoft Office applications, particularly Excel for data analysis, reporting, and visualization.