Process Validation Engineering Co-Op

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 Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible impact.

Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers 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 youll help bring life-changing innovations to lifeimpacting millions around the world. We bring together deep scientific expertise an unwavering commitment to quality and a collaborative spirit to drive progress. Whether youre 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 potentialone 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 Bachelors 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 its 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 well accelerate the real-life impact of tomorrows 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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