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 Lead Trainer and Document Specialist position is part of Gene Processing located at 2600 Crosspark Rd.
Coralville, IA location 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.
Shift: Monday - Friday 8:00AM - 5:00/4:30PM
In this role, you will have the opportunity to:
Create and maintain department and process specific work instructions, SOPs, processing aids, and other QMS documentation needed to support department functions.
Create and maintain department and role specific training plans.
Coordinate department training activities, training feedback, and support training record accuracy via QMS.
Coordinate and document equipment, process, and software validation activities effectively.
Perform controlled copy and internal reference document audits.
Serve as a representative for department during internal and customer audits.
Support product and process quality documentation within the QMS including process changes, process or product deviations, product or process non-conformances, and quality investigations.
The essential requirements of the job include:
An associate degree in a science-related field (biology, chemistry, etc.
) and 2 years of related experience or equivalent combination of education and experience.
Bachelor’s degree in a science related field preferred.
Ability to coordinate and document equipment, process, and software validation activities effectively.
Ability to perform controlled copy and internal reference document audits and serves as a representative for department during internal and customer audits.
Proficiency in supporting product and process quality documentation within the QMS including process changes, process or product deviations, product or process non-conformances, and quality investigations.
It would be a plus if you also possess previous experience in:
Experience with sequencing data preferred.
PCR and cloning experience preferred.
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.
At Danaher we bring together science, technology and operational capabilities to 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.
Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond.
For more information, visit www.
danaher.
com.
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