Quality Assurance Technician II

doTERRA International LLC•Pleasant Grove, UT

1d•Onsite

About The Position

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 Title: Quality Assurance Technician II Department: Quality Assurance Reports to: Supervisor, Quality Assurance

Requirements

Two year’s acceptable performance as Technician I or equivalent experience.
2-5 years of QA Tech experience in a food juice, dietary supplement, device or drug facility.
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. Must be able to identify small defects.
Excellent communication skills in writing, listening, and responding with feedback within quality and production.
Strong organizational abilities.
Basic computer skills; data entry, Microsoft Office suite required.

Nice To Haves

Associate’s or Bachelors preferred.
Bilingual Spanish and English preferred.

Responsibilities

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 Supervisor for dispositions; assists in making corrective measures.
Assist in non-conformance investigations.
Performs materials and product inspections and releases; document review and approval, identification and communication to management of non-conforming materials and products; cGMP compliance.
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. Complete associated logs.
Performs batch record review and approval as outlined to product specification.
Performs, monitors and documents 1st article inspection and in-process checks in 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.
Assists with on the job training for production and quality staff regarding quality requirements.