Quality Supervisor - Off-Shift

Kdc One; Groveport, Northern (OH, KY); Hybrid; USD 70,000 - 90,000; Full time

Job summary

Kdc One is seeking a Quality Supervisor for an off-shift on-site role in Groveport, OH. You will lead a QA/QC team to ensure products meet GMP and FDA standards, driving issue resolution and continuous improvement.

The position requires a Bachelor’s in a related science and 3+ years of supervisory experience in lab settings, preferably cosmetics or pharmaceuticals, with a strong compliance mindset and ability to lead cross-functional efforts.

Qualifications

• Lead a team of QA/QC professionals to meet production goals with GMP/FDA standards.
• Investigate quality issues and implement timely resolutions.
• Conduct root cause analyses and preventive actions.
• Support audits and ensure documentation for launches and transfers.

Responsibilities

• Lead with purpose and inspire QA/QC teams.
• Tackle quality issues and provide expert guidance.
• Drive continuous improvement and corrective actions.
• Champion compliance and documentation accuracy.
• Develop talent and coach team members.
• Collaborate with Customer Service, Engineering, and Production.

Skills

Leadership

GMP knowledge

Root cause analysis

Problem-solving

Team coaching

Collaboration

Education

Bachelor’s degree in Chemistry/Microbiology/Biology

Tools

Laboratory workflows

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.