What are the responsibilities and job description for the Quality Lead Technician position at Canyonside Labs LLC?
POSITION TITLE: Quality Lead 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 overseeing quality processes within our NSF
455-2 compliant dietary supplement facility. This role ensures that 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.
2
DUTIES:
? Identify and pursue new business opportunities within supplement industry
? 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-ofspecification (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:
? 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
3
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.
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 overseeing quality processes within our NSF
455-2 compliant dietary supplement facility. This role ensures that 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.
2
DUTIES:
? Identify and pursue new business opportunities within supplement industry
? 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-ofspecification (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:
? 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
3
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.
