Quality Supervisor - Off-Shift

About the role

KDC is a network of best-in-class custom formulators and manufacturers of color cosmetics, skincare, haircare, bath & body, fragrance, deodorant, home, health, industrial, and auto care products. KDC delivers high-touch innovation, operational excellence, and speed to market to well-known and emerging beauty, personal, and specialty companies from coast to coast. KDC has its head office in Longueuil, Québec. In addition, KDC has 10 operating facilities located throughout North America. Altogether, the company employs nearly 4,800 talented and dedicated employees in North America. 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.

Responsibilities

• 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.

Requirements

• 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.

Skills

• A natural leader with exceptional problem-solving skills, adaptability, and the ability to thrive under pressure.

Benefits

• 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.

Schedule

Full-Time, 6:00pm‑4:00am (off‑shift). On‑site in Groveport, OH.