QC Analyst II

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.

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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:

• Bachelors 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 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.

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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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