Analyst I QC GMP

At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences.

Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

This role is a first shift position with the hours being 8am-5pm, Mon-Fri.

This position is part of the Quality and Regulatory Affairs department located in Fargo, ND, and will be onsite working a first-shift position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Team and report to the QC Lab Manager. The QC Analyst I activities include but are not limited to developing and implementing testing, sampling, and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met.

In this role, you will have the opportunity to:

• Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments.

• Accurately generate and record raw data and analyze, as well as calculate, interpret, and trend the results while adhering to GMP Standards.

• Document and compare testing results against control/specification limits.

The essential requirements of the job include:

• Experience working in a laboratory environment is preferred, not required.

• Bachelor’s degree in a science related field is required.

• Knowledge of basic laboratory practices, including an in-depth knowledge of biological processes.

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

• Working in a GMP or Clinical Laboratory Environment.

• Biotech-related Quality Control Laboratory.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to use hands, stand, sit, and bend.

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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. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [email protected] to request accommodation.