QA Supervisor - Raw Materials

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: Supervision of QA Technicians, monitoring of GMP compliance with recommendations for corrective measures; involvement and direct supervision in all area quality activities.
Reviews and recommends approvals for deviations, QA holds, rework, and in-process adjustments.
Investigates non conformances, deviations and CAPA and elevates issues to MRB as needed Reviews and approves finished product specifications and raw material specifications.
Reviews and approves master manufacturing and production batch records Signs as final product release for all components, raw materials, bulk and finished goods Audits dietary supplement, component and raw material suppliers as needed Ensures collaborative process development, continuous improvement and problem solving with quality control, production, maintenance and warehouse Oversees the facility’s calibration control program.
Works with and supports Operation functions.
Involved and is part of the FDA, NSF, TGA, KFDA etc.
audit response team.
Supervises the activities of Quality Technicians and the Quality Assurance Leads/Supervisors Prepares weekly, monthly and quarterly reports by collecting, analyzing, trending and summarizing deviations, QA holds, rework, etc.
; submits regular reports to Quality Assurance Director.
Complies with FDA, cGMP and other requirements and enforcing adherence to requirements.
Signs as an authorized person for release for supply of product.
Job Qualifications Familiar with dietary supplement, food and cosmetic regulations 3 to 5 years of supervisory experience required in QC/QA environment B.
S.
in any related scientific field or equivalent experience Ability to perform and review all quality processes from receiving to shipping of product.
Knowledgeable in Quality Control, Assurance and Document Control functions/processes.
Knowledge in label control Quality functions.
Knowledge in retain room process.
Knowledge in Microbiology testing and GC-MS chemical analysis.
Ability and knowledge in performing in-house audits.
Knowledge and experience with applicable FDA regulation, cGMP requirements and GLP requirements.
Ability to write and implement standard operating procedures in the warehouse and corporate facilities.
Ability to understand, monitor and review all Quality processes in the warehouse and corporate facilities Familiarity with basic computer programs….
i.
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WORD, EXCEL, ACCESS Other duties as assigned by Manager 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.