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Quality Technician

Plant Therapy LLC
Twin Falls, ID Full Time
POSTED ON 4/12/2025
AVAILABLE BEFORE 6/11/2025

POSITION TITLE:     Quality Technician     

 

REPORTS TO:          Quality Manager

 

COMPANY DESCRIPTION:

Canyonside Labs specializes in the custom manufacturing of dietary supplements - capsules, liquids and powders. Through superior customer service, exceptional quality, short lead times and competitive pricing, Canyonside Labs is the industry-leading manufacturing partner for small to mid-sized brands. Canyonside Labs is committed to producing high-quality, safe, and compliant products. As an NSF 455-2 certified facility, we follow strict regulatory standards to ensure product integrity, safety, and consistency.

QUALIFICATIONS:

  • Associate’s or Bachelor’s degree in Chemistry, Biology, Food Science, or a related field preferred (or equivalent industry experience).
  • 2-4 years of experience in quality control within a manufacturing environment.
  • Experience with quality testing methods, COA verification, and in-process inspections.
  • Strong attention to detail and ability to interpret quality data and specifications.
  • Proficiency in maintaining accurate documentation and batch records.
  • Basic understanding of laboratory instruments and calibration procedures.
  • Good communication skills and ability to collaborate with cross-functional teams.
  • Proficiency in Google Suite (Google Sheets, Docs) or equivalent software for data entry and reporting.

JOB SUMMARY:  

The Quality Lead is responsible for executing and facilitating quality processes within our NSF 455-2 compliant dietary supplement facility. This role ensures raw materials, in-process products, and finished goods meet all established specifications and regulatory requirements. The Quality Lead works closely with Production, Regulatory and Supply Chain teams to ensure compliance with NSF 455-2, 21 CFR Part 111 (GMP), and FDA regulations preferred.

 

DUTIES:

  • Conduct routine laboratory and visual inspections of raw materials, in-process products, and finished goods to ensure compliance with specifications.
  • Review and validate supplier Certificates of Analysis (COAs) for accuracy and compliance with quality standards.
  • Monitor and document in-process quality checks during encapsulation and bottling, ensuring adherence to GMP, NSF 455-2, and internal quality control standards.
  • Assist in label reconciliation and packaging verification to ensure accuracy and regulatory compliance.
  • Prepare and submit product samples for third-party laboratory testing, maintaining proper Chain of Custody (CoC) documentation.
  • Identify, document, and report quality deviations, non-conformances, and out-of-specification (OOS) results.
  • Conduct swab tests and sanitation monitoring to verify compliance with GMP sanitation standards.
  • Monitor and track raw materials, work-in-progress (WIP), and finished goods to ensure compliance with quality standards and regulatory requirements.
  • Maintain detailed logs, batch records, and test results in compliance with GMP and NSF 455-2 documentation requirements.
  • Adhere to and enforce quality control policies in accordance with NSF 455-2, 21 CFR Part 111, and FDA regulations.
  • Collaborate with Quality Assurance, Production, and Warehouse teams to ensure consistent quality and compliance.

PREFERRED SKILLS:

  • Highly self-motivated individual who is comfortable working individually while managing multiple tasks efficiently to meet defined deadlines.
  • Must be able to operate lab instruments needed for chemistry, microbiological analysis.
  • Experience working in an NSF-certified or FDA-regulated facility.
  • Understanding of laboratory testing and environmental monitoring programs.
  • Experience with CAPA (Corrective and Preventive Action) investigations.
  • Knowledge of supplier qualification and vendor audits.

 

WORK LOCATION:  Onsite only

 

HOURS:  Standard Day Shift hours - Monday-Friday

 

WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS:

  • Work in a dietary supplement manufacturing facility, including production and laboratory environments.
  • Ability to stand, sit, or walk for extended periods.
  • Occasionally lift and move objects up to 50 lbs.
  • Work in temperature-controlled or production areas.
  • Use of Personal Protective Equipment (PPE) as required.

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