QA Document Control Specialist I

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.

Job Description:

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.

Job Responsibilities:

• Controls, routes, and files product specifications in Master Control

• Controls, routes, reviews, and edits company forms

• Responsible for routing documents and change control forms for approval

• Maintains and updates other controlled documents as assigned

• Maintains archived records and the document library

• Trains document users on document control practices

Job Qualifications:

• Associates or BA/BS degree preferred

• Experience in Electronic Quality Management System (eQMS), Master Control, SAP, etc.

• Prefer document control experience in a regulated environment e.g. dietary supplement, pharmaceutical, 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, filling 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 s

• Possess excellent computer (MS office: word; excel; access; outlook), writing and editing skills

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.