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.
Performs inspections, sampling, auditing, and documentation reviews to ensure compliance with quality standards. Coordinates with manufacturing personnel for best practices; communicates non-conforming circumstances to Quality Managers for dispositions; assists in making corrective measures.
- Performs incoming AQL inspection on raw materials/finished goods/components according to written standard operating procedures, work instructions and specifications in Receiving.
- Responsible for pulling and submitting a representative sample for at least identity and microbial testing.
- Approves and releases incoming coming raw materials/finished goods/components.
- Verifies and performs checks on cleaning processes as established in procedures pertaining to operation area before, during and after production.
- Performs batch record review and approval as outlined to product specification.
- Performs, monitors and documents 1st article inspection and in-process checks in batching, mixing and filling rooms in operation area.
- Verifies calibration and verifications on equipment logs in operation area.
- Responsible for pulling in-process and finished good samples for QC testing to verify purity, identity, specificity and conformance to product specification. Responsible for performing AQL inspection on finished product.
- Responsible for reviewing and releasing finished product for shipping.
- Responsible for label control; process for received and released labels from Quarantine are followed.
- 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.
- Two year's acceptable performance as Technician I or equivalent experience.
- Knowledge and experience with applicable FDA regulation and cGMP requirements required.
- High School Diploma or GED required.
- Attention to detail and organization of tasks and workloads.
- Excellent communication skills in writing, listening, and responding with feedback.
- Strong organizational abilities.
- Bi-lingual English and Spanish preferred.
- 2-5 years QA Technician experience in a food, juice, dietary supplement, medical device, or drug facility.
- Long periods of standing, bending, and repeated lifting (2-5 lbs)
- Must be able to handle moderate noise level (<75db)
- Must be able to work in manufacturing environments (clean rooms and warehouse)
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.