Specialist, Therapeutics QC

Integrated DNA Technologies (IDT) is the leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.IDT 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 position is part of the Genomics Medicine, Quality Control Department located in Coralville, IA and will be onsite. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things

In this role, you will have the opportunity to:

• Analyzes data and information for quality, consistency, and accuracy.

• Handles sample and reagent preparations for required assays in a careful manner., troubleshoots and corrects problems that occur during daily operations.

• Programs, operates, maintains and troubleshoots a variety of equipment including sample handling equipment and other general laboratory equipment and seeks assistance when necessary.

The essential requirements of the job include:

• Associate Degree in science, engineering, or related field

• Minimum of 1 year experience with quality control of oligonucleotides with demonstrated skills in quality system procedures such as change control, deviation, nonconformance, and good documentation practices

• Strong experience with two or more of the following: LCMS for raw materials or finished oligos, Capillary Electrophoresis, GC, Karl Fischer, titrations, general microbiology.

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

• Bachelor Degree in science, engineering, or related field

• Experience in a GMP environment and experience with 21 CFR 210 & 211 and ICH Q7

• Experience performing method validation and writing SOP’s

This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

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.

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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.