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.
This position completes all documentation services for manufacturing and quality systems, including change control, technical writing, maintenance of records, and compliance with GMP documentation practices.
Reviews, approves, and controls company standard operating procedures, forms, labels, specifications, etc. in an electronic Quality Management System (eQMS) like Master Control, SAP, etc.
Responsible for routing documents and change control forms for approval
Responsible for updating and maintaining the following logs: MDA's; MRB's, OOS's; SCN's, CAPAs
Responsible for tracking due dates and extensions for CAPA reports and filing the completed reports
Maintains and updates other controlled documents as assigned
Maintains archived records and the document library
Trains document users on document control practices.
Associates or BA/BS degree preferred
Must have 2-4 years of document control experience in a regulated environment e.g. dietary supplements, pharmaceuticals, blood products, juice or medical device
Must be extremely detail-oriented
Must be able to work well with others especially when editing or revising their work products
Must be willing to perform repetitious tasks such as updating forms, filing logs, copying and scanning documents
Possess excellent computer (MS office: word; excel; access; outlook), writing, and editing skills
Must be willing and able to spend 6-8 hours per day standing and filing and/or sitting and performing computer-based tasks
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.
Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!Apply Online