The board
- Hours
- Full time
- Where
- Fargo, North Dakota, United States
- Posted
- Sep 2
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.
What you'd do
- 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.
- 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.
- 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.
- Starts
- 2026-09-01