Evening QA Supervisor — FDA‑Regulated Manufacturing

Nutramax Laboratories, Inc.; Lancaster (SC); On-site; USD 65,000 - 90,000; Full time

Job summary

Nutramax Laboratories, Inc. in South Carolina is seeking a QA Supervisor to oversee QA Inspectors, Label Issuance, and Team Leads, ensuring product quality and regulatory compliance.

The role reports to the QA Assistant Manager and involves reviewing SOPs, NCRs, deviations, and coordinating with Production and R&D to maintain cGMP standards. Hours are Monday–Friday, 3:15 pm to 11:30 pm, with shift flexibility as needed.

Qualifications

• Minimum 4–5 years in an FDA-regulated manufacturing environment with at least 3 years in QA/QC.
• Prior FDA or equivalent inspection experience is highly recommended.

Responsibilities

• Supervise QA Inspectors, Label Issuance, and Team Leads.
• Monitor QA and production processes and ensure adherence to cGMPs and regulations.
• Review and approve protocols and SOPs; support investigations and deviations.
• Coordinate with Production, NPD, and other departments to maintain Quality Systems.

Skills

Communication

Supervisory experience

Education

High School Diploma

AA/BS preferred

Job description

Nutramax Laboratories, Inc. in South Carolina is seeking a QA Supervisor to oversee QA Inspectors, Label Issuance, and Team Leads, ensuring product quality and regulatory compliance.

The role reports to the QA Assistant Manager and involves reviewing SOPs, NCRs, deviations, and coordinating with Production and R&D to maintain cGMP standards. Hours are Monday–Friday, 3:15 pm to 11:30 pm, with shift flexibility as needed.