Origin: a Latin derivative
meaning "Gift of the Earth."
At doTERRA we encourage all employees to seek out opportunities that will expand their skill set. We strive to help achieve personal career goals by providing opportunities of growth and movement throughout the company.
Reports deviations, product, and in-process issues to Quality management.
Works with and supports Operation functions which involve Quality.
Complies with FDA, cGMP and other requirements and enforcing adherence to requirements.
Assists with complaint and CAPA investigations.
Assists with review and evaluation of process and equipment verifications and validations.
Assists with the development of procedures and forms.
Serves as back up to QA supervisor and QA techs as needed.
Works closely with operations supervisors and leads to ensure collaborative problem solving as issues arise.
Reports reworks, deviations, product, and in-process issues to Quality management.
Verifies calibration and verifications on equipment logs in operation area.
Performs batch record review and approval as outlined to product specification.
High School Diploma or GED required.
Two year's acceptable performance as Technician I or equivalent experience.
Knowledge and experience with applicable FDA regulation and cGMP requirements required.
Attention to detail and organization of tasks and workloads.
Excellent communication skills in writing, listening, and responding with feedback within quality and production. Must be good at negotiation and conflict resolution.
Strong organizational abilities.
Long periods of standing, bending, and repeated lifting (2-5 lbs)
Moderate noise level (<75db)
We are currently accepting applications for this position.
doTERRA International, LLC. is committed to employing a diverse workforce. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, protected veteran status, or disability.