Quality Assurance Supervisor - Off-Shift

kdc/one, Groveport; Groveport (OH); On-site; USD 70,000 - 90,000; Full time

Job summary

kdc/one is seeking a Quality Supervisor in Groveport, OH to lead a QA/QC team, uphold GMP and FDA standards, and ensure products meet quality.

You will investigate issues, drive corrective actions, and collaborate with Production, Engineering, and Customer Service to deliver compliant launches.

This on-site role offers opportunities to mentor staff and advance within the company.

Qualifications

• Bachelor's degree in Chemistry, Microbiology, Biology, or related science.
• 3+ years of supervisory experience in laboratory environments.
• Strong knowledge of GMP, FDA regulations, and microbiological testing.
• Leadership under pressure with adaptive decision making.

Responsibilities

• Lead a team of QA and QC professionals to meet production goals.
• Investigate quality issues and implement corrective actions.
• Drive continuous improvement through root cause analysis.
• Audit readiness and ensuring documentation for launches and transfers.
• Coach, mentor, and develop lab staff.
• Collaborate cross-functionally with Customer Service, Engineering, and Production.

Skills

Quality leadership

GMP compliance

FDA regulations

Root cause analysis

Problem solving

Education

Bachelor's degree in Chemistry, Microbiology, Biology, or related science

Job description

Quality Supervisor

Location: Groveport, OH | Full-Time | 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, 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.