Night QA Supervisor - FDA/GMP Leader (3rd Shift)

Kelly Services; Lancaster (SC); On-site; USD 75,000 - 85,000; Full time

Benefits offered by this job

Annual bonus opportunity

Job summary

Kelly Services seeks a Quality Assurance Supervisor for 3rd shift in Lancaster, SC, leading an overnight QA team. The role oversees QA personnel, ensures cGMP compliance, and supports manufacturing operations while driving continuous improvement.

The ideal candidate has 4–5+ years in FDA-regulated environments, strong leadership, and hands-on quality systems experience. Salary is $75,000–$85,000 with an annual bonus opportunity.

Qualifications

• Associate’s or Bachelor’s degree in a science-related field preferred.
• 4–5+ years of experience in an FDA-regulated manufacturing or production environment.
• At least 3 years of Quality Assurance experience.

Responsibilities

• Supervise, coach, and develop Quality Assurance personnel on 3rd shift.
• Provide QA oversight for manufacturing, packaging, and warehouse operations.
• Review batch records, production documentation, and quality records for accuracy and compliance.
• Lead investigations involving deviations, non-conformances, and quality events; drive CAPA.
• Partner with Manufacturing, Quality Control, and cross-functional teams to resolve issues.
• Ensure compliance with FDA regulations, cGMP, SOPs, and company standards.
• Support internal audits, regulatory inspections, and inspection readiness.
• Train employees on GMP requirements and quality systems.
• Monitor quality metrics and drive continuous improvement.

Skills

Leadership

Quality assurance

Communication

Problem solving

Education

Associate’s or Bachelor’s degree in a science-related field

Tools

Batch record review

CAPA investigations

Lean Manufacturing

ISO standards

Job description

Kelly Services seeks a Quality Assurance Supervisor for 3rd shift in Lancaster, SC, leading an overnight QA team. The role oversees QA personnel, ensures cGMP compliance, and supports manufacturing operations while driving continuous improvement.

The ideal candidate has 4–5+ years in FDA-regulated environments, strong leadership, and hands-on quality systems experience. Salary is $75,000–$85,000 with an annual bonus opportunity.