Process Validation Engineering Co-Op
About The Position
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.
Requirements
- 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.
- Ability to lift, move or carry items up to 10lb.
Nice To Haves
- Exposure to GMP-regulated environments, process validation, equipment qualification, media fills (APS), CCIT, cleaning validation, or process monitoring activities.
- Experience with statistical analysis and data visualization tools such as JMP or Minitab.
- Following cellular process steps within a lab under GLPs.
Responsibilities
- 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.
Benefits
- Health care program
- Paid time off
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What This Job Offers
Career Level
Intern
