Job Description

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 and Supervisor for dispositions; assists in making corrective measures. Assist in non-conformance investigations.

Responsibilities:     

  • Responsible to review doTERRA products and manufacturing process for compliance to State and Federal regulations, with a focus on compliance to cGMP’s for TGA, OTC drugs, TGA and NHP’s.

  • Frequent interaction with production, planning and vendor managers to ensure company standards for product quality are adhered to and timelines for product releases are kept within goal.

  • Responsible to perform annual product reviews for drug products.

  • 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.

  • 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.

Job Qualifications:

  • 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. Associate’s or Bachelors preferred.

  • 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.

  • Bilingual Spanish and English preferred.

  • Basic computer skills; data entry, Microsoft Office suite required.

Work Environment:

  • Long periods of standing, bending, and repeated lifting (35-45 lbs)

  • Moderate noise level (<75db)

  • Manufacturing environment (clean rooms and warehouse)

  • Extended periods filing and moving file boxes

We are currently accepting applications for this position.

Position Level: 
Function:                            Quality Assurance - MFG
Type:Full-Time
Shift:Swing
Requisition ID:25092
Location:
 Pleasant Grove, Utah, 84062 

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.

Application Instructions

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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