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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 (https://danaher.com/our-businesses) 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 (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible.

The Analyst II, Quality Control is responsible for performing a broad range of protein QC assays to support manufacturing, stability, and method validation. The Analyst II is responsible for executing laboratory tasks in accordance with standard operating procedures and performing basic equipment maintenance and calibration.

This position reports to the Quality Control Supervisor and is part of the Quality Control Group located in Madison, Wisconsin and will be an on-site role.

In this role, you will have the opportunity to:

+ Independently perform routine QC assays for biological macromolecules (Concentration, Purity, Activity, Residual, Compendial) according to established standard operating procedures under direction from the QC Supervisor

+ Perform data entry and review own work and peers’ work for accuracy in accordance with laboratory and Good Documentation Procedures

+ Document and compare testing results against control/specification limits, and report all Out of Specification (OOS), Out of Trend (OOT) results and other quality concerns to the QC Supervisor.

The essential requirements of the job include:

+ Bachelor’s degree in Scientific field + 2 years of experience working in an ISO 13485 and/or GxP laboratory environment

+ Knowledge of analytical laboratory practices and Good Documentation Practices

+ Have good depth perception, manual dexterity ability, and steady hands for pipetting

It would be a plus if you also possess previous experience in:

+ Prior experience with one or more of: HPLC, 96-well plate assays, CE-SDS, ELISA, qPCR

+ Electronic Laboratory Information Management Systems (LIMS)

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 (https://leplb1040.upoint.alight.com/ah-angular-afirst-web/#/web/danaher/cp/preauth-home) .

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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.

For more information, visit www.danaher.com .

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here (http://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) .

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [email protected] .