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:
Performs documentation creation, auditing, and documentation reviews to ensure compliance with quality standards.
Coordinates with manufacturing personnel for best practices; communicates non-conforming circumstances to Quality Lead for dispositions; assists in taking corrective measures.
Assist in non-conformance investigations.
Job Responsibilities:
Creates, obtains approvals, and reviews master manufacturing records, production batch records, indexes, and logs
Maintains records in an orderly and easily retrievable manner
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
Approve and release incoming 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 in the product specification
Performs, monitors, and documents 1st article inspection and in-process checks in filling rooms in the operation area
Verifies calibration and verifications on equipment logs in the 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 the finished product.
Responsible for reviewing and releasing the finished product for shipping
Responsible for label control; the process for received and released labels from Quarantine is followed
Reports deviations, product, and in-process issues to Quality management
Works with and supports Operation functions that involve Quality
Complies with FDA, cGMP, and other requirements and enforces adherence to requirements
Assists with on-the-job training for production and quality staff regarding quality requirements
Other Responsibilities as assigned
Job Qualifications:
1-2 years of QA experience preferred
Knowledge and experience with applicable FDA regulations 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 to feedback
Must be able to handle moderate noise levels (<75db)
Must be able to work in manufacturing environments (clean rooms and warehouse)
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.
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