On-Site QA Lead — Dietary Supplements

Lief Labs; California; On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

401(k) with Company Participation

Life Insurance

Education Reimbursement Program

Paid Time Off (PTO)

Job summary

Lief Labs is hiring a Quality Assurance Inspector Lead for an on-site, first-shift role in Santa Clarita, CA. You will guide QA Inspectors on the manufacturing floor, ensure inspections and releases meet FDA 21 CFR Part 111 cGMP standards, and collaborate on deviations and CAPA actions.

Responsibilities include reviewing batch records, supporting audits, and updating quality procedures while maintaining safety protocols in a fast-paced dietary supplements environment.

Qualifications

• High school diploma or equivalent required.
• Associate or bachelor’s degree in a scientific/technical field preferred.

Responsibilities

• Lead daily QA activities for Inspectors and provide on-the-floor guidance.
• Inspect raw materials, in-process products, and finished goods; execute line clearances.
• Verify labels, components, reconciliations, and product quality with appropriate equipment and methods.
• Document results, deviations, and nonconformances.
• Monitor blending, encapsulation, tableting, coating, packaging, and labeling in real time.
• Review batch records and quality documents for accuracy and cGMP compliance.
• Maintain inspection and test records and support Certificates of Analysis.
• Identify process improvements and support root-cause analysis, CAPA actions.
• Train staff on quality standards and inspection methods.
• Support internal and external audits and change control processes.
• Assist deviations, nonconformance reports, and material disposition.

Skills

Attention to detail

Documentation

Communication

Problem solving

Education

High School Diploma or Equivalent

Assoc. or Bachelors in scientific/technical field preferred

Job description

Lief Labs is hiring a Quality Assurance Inspector Lead for an on-site, first-shift role in Santa Clarita, CA. You will guide QA Inspectors on the manufacturing floor, ensure inspections and releases meet FDA 21 CFR Part 111 cGMP standards, and collaborate on deviations and CAPA actions.

Responsibilities include reviewing batch records, supporting audits, and updating quality procedures while maintaining safety protocols in a fast-paced dietary supplements environment.