Quality Supervisor - Off-Shift

Kdc One; Madison Township (OH); On-site; USD 70,000 - 95,000; Full time

Job summary

Kdc One in Groveport, OH is seeking a Quality Supervisor for the Off-Shift to lead a QA/QC team in a fast-paced manufacturing environment. You will ensure products meet GMP and FDA standards, resolve quality issues, and drive continuous improvement on the production floor.

You’ll collaborate with Customer Service, Engineering, and Production, coach staff to develop skills, and participate in audits and new product launches while maintaining documentation integrity and compliance throughout

Qualifications

• 3+ years of supervisory experience in laboratory environments.
• Experience in cosmetics or pharmaceuticals preferred.
• GMP and FDA regulations knowledge required.
• Strong problem-solving and adaptability under pressure.

Responsibilities

• Lead and inspire a QA/QC team to meet production goals with GMP/FDA standards.
• Investigate quality issues and provide timely resolutions.
• Conduct investigations and root cause analyses for quality improvements.
• Participate in audits and ensure documentation for launches/transfers.
• Coach, mentor, and develop team to achieve excellence.
• Collaborate with Customer Service, Engineering, and Production to ensure seamless operations.

Skills

Team leadership

GMP knowledge

FDA regulations

Root cause analysis

Problem solving

Cross-functional collaboration

Education

Bachelor’s degree in Chemistry

Job description

Quality Supervisor – Off-Shift

Location: Groveport, OH | Full-Time, 6:00pm-4:00am | On-Site

Lead Quality. Drive Excellence. Make an Impact.

Are you ready to take charge and make a real difference in a fast-paced, dynamic environment? As our Quality Supervisor – Off-Shift, you’ll be the driving force behind ensuring every product meets the highest standards of quality and compliance. This is your opportunity to lead a talented team, solve complex challenges, and play a critical role in delivering products that customers trust.

What You’ll Do

• Lead with Purpose: Manage and inspire a team of QA and QC professionals to meet production goals while upholding GMP and FDA standards.
• Be the Problem-Solver: Tackle quality issues head-on, provide expert guidance, and ensure timely resolutions that keep operations running smoothly.
• Drive Continuous Improvement: Conduct investigations, root cause analyses, and implement corrective actions to elevate quality performance.
• Champion Compliance: Participate in audits, refine processes, and ensure documentation is flawless for new product launches and transfers.
• Develop Talent: Coach, mentor, and empower your team to achieve excellence and grow professionally.
• Collaborate Across Functions: Work closely with Customer Service, Engineering, and Production to ensure seamless operations and exceptional outcomes.

What We’re Looking For

• A Bachelor’s degree in Chemistry, Microbiology, Biology, or related science.
• 3+ years of supervisory experience and hands‑on expertise in laboratory environments—preferably cosmetics or pharmaceuticals.
• Strong knowledge of GMP, FDA regulations, and microbiological testing methodologies.
• A natural leader with exceptional problem‑solving skills, adaptability, and the ability to thrive under pressure.

Why You’ll Love It Here

• Impact: Your work ensures product integrity and customer satisfaction.
• Growth: Opportunities to lead, innovate, and advance your career.
• Culture: A collaborative, safety-focused environment where your ideas matter.
• Challenge: Every day brings new opportunities to learn and make a difference.

Physical & Work Environment

• Climate-controlled facility with moderate to loud noise levels.
• Ability to lift up to 50 lbs occasionally and navigate a busy production floor.

Join us and be the quality champion who sets the standard for excellence.