Quality Supervisor - Off-Shift

KDC One • Groveport, OH

1d • Onsite

About The Position

The Quality Supervisor – Off-Shift leads QA and QC professionals in an on-site, fast-paced production environment. The role is responsible for ensuring products meet quality and compliance standards, including GMP and FDA requirements. The supervisor resolves quality issues, drives investigations and corrective actions, supports audits and documentation, develops team members, and collaborates with Customer Service, Engineering, and Production.

The position is based in Groveport, Ohio, and works full-time from 6:00 p.m. to 4:00 a.m. The facility is climate-controlled, with moderate to loud noise levels; the role involves navigating the production floor and occasionally lifting up to 50 pounds.

Requirements

• Bachelor’s degree in Chemistry, Microbiology, Biology, or a related science.
• At least 3 years of supervisory experience.
• Hands-on expertise in laboratory environments.
• Strong knowledge of GMP and FDA regulations.
• Knowledge of microbiological testing methodologies.
• Problem-solving skills, adaptability, and ability to thrive under pressure.

Nice To Haves

• Laboratory experience in cosmetics or pharmaceuticals.

Responsibilities

• Manage and inspire a team of QA and QC professionals to meet production goals while upholding GMP and FDA standards.
• Address quality issues, provide expert guidance, and ensure timely resolution.
• Conduct investigations and root cause analyses, and implement corrective actions to improve quality performance.
• Participate in audits, refine processes, and ensure documentation is complete for new product launches and transfers.
• Coach, mentor, and empower team members to support their professional growth.
• Collaborate with Customer Service, Engineering, and Production to support smooth operations and strong outcomes.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager