Description
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 Quality Control Development department located in Coralville, IA and will be on-site. 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:
+ Independently design, execute, and/or oversee execution of method development and validation for QC processes to be implemented in a production QC department.
+ Independently author relevant documentation including method development, characterization, method validation procedures, SOPs, and analysis documents to be used in the production QC departments, following QA/RA guidelines
+ Create and execute project timelines on cross-functional strategic projects, ensuring timely delivery of milestones, and providing leadership to extended team members as needed
+ Acts as a mentor and trainer for QC Development Scientists; leads training and onboarding activities for colleagues with less experience
+ Applies extensive scientific knowledge and laboratory skills to independently execute complex bench experiments using a variety of molecular biology and/or analytical techniques as directed, while maintaining GLP
The essential requirements of the job include:
+ Bachelor’s degree in a science related field required
+ 5+ years of experience working with relevant QC techniques (Mass Spectrometry and/or HPLC) is required
+ Demonstrated experience in QC method development, new product development, process improvement implementation required
+ Experience working in a GLP-compliant laboratory environment, including accurate and thorough documentation in lab notebooks required
+ Demonstrated experience in written and verbal communication to a wide variety of audiences required
It would be a plus if you also possess previous experience in:
+ Experience with project management tools and techniques preferred
+ Experience with statistical analysis and experimental design tools (JMP, SAS, R, DOE, etc.) preferred
#LI-MF2
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 (https://www.dol.gov/agencies/ofccp/posters) .
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 applyassistance@danaher.com to request accommodation.
