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.
Travel, Motor Vehicle Record & Physical/Environment Requirements:- Ability to lift, move or carry items up to 10lb.
It would be a plus if you also possess previous experience in:- 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.
The hourly rate for this role is $30.00. This is the rate that we in good faith believe is the rate of compensation for this role at the time of this posting
Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we'll 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.
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