QA Tech I

doTERRA International LLC•Pleasant Grove, UT

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 Description: Materials and product inspections and releases; document reviews and approval, pulling of samples, reporting of nonconformance, monitoring of GMP compliance.

Requirements

1-2 years QA experience preferred
Knowledge and experience with applicable FDA regulation and cGMP requirements required.
High School Diploma or GED required.
Excellent communication skills in writing, listening, and responding with feedback.
Ability to multi-task, set priorities and manage time effectively
Critical thinking and problem-solving ability
An ability and a willingness to adapt to a changing work environment
An ability to work to repetition
Long periods of standing, bending, and repeated lifting (2-50 lbs)
Must be able to handle moderate noise level (<75db)
Must be able to work in manufacturing environments (clean rooms and warehouse)

Responsibilities

Performs inspection on raw materials and components according to written standard operating procedures, work instructions and specifications in Receiving.
Verifies and performs checks on cleaning processes as established in procedures pertaining to operation area before, during and after production.
Performs batch record review as outlined to product specification.
Performs, monitors and documents 1st article inspection and in-process checks in batching,
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 obtaining retain samples, logging of samples and placement into storage.
Responsible for performing AQL inspection on finished product.
Responsible for verifying cleaning procedures on Glass and Brittle Plastic breakage incidents and segregating any affected finished products/components/raw materials.
Responsible for monitoring Blood and Other Body Fluid Cleanup, according to written standard operating procedures.
Responsible for monitoring and recording temperature controls throughout the building.
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.
Perform other duties as assigned by QA Management.