Off-Shift Quality Supervisor

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

Benefits offered by this job

Competitive salary with annual incentive

Health, Vision, Dental, 401k

Paid time off and holidays

Opportunities for career advancement

Job summary

Kdc/one is expanding and seeks an experienced Off-Shift Quality Supervisor in Groveport, OH. This role oversees QA and QC teams, ensuring compliance with GMP and FDA standards while managing production quality and timelines. Ideal candidates have a Bachelor's degree in a relevant science and significant supervisory experience.

Qualifications

• 3+ years of supervisory or lead experience.
• Experience with laboratory equipment, aseptic sampling, and microbiological testing in cosmetics or pharmaceuticals.

Responsibilities

• Manage off-shift QA and QC teams to meet production schedules.
• Lead inspections and resolve quality-related issues.
• Assist in audits and develop corrective actions.

Skills

Supervisory Skills

Quality Assurance

Quality Control

Problem Solving

Communication

Education

Bachelor’s degree in Chemistry, Microbiology, Biology, or related science field

Job description

Join to apply for the Off-Shift Quality Supervisor role at kdc/one, Groveport.

Kdc/one is currently growing, and we are looking for an experienced Off-Shift Quality Supervisor as part of the kdc/one network. We are a leading producer of beauty and personal care products!

This role supervises, organizes, directs, and measures all activities performed by the off-shift Quality Assurance (QA) and Quality Control (QC) teams to ensure that production schedules are met and products are released in accordance with GMP and FDA standards, supporting customer satisfaction and financial goals.

Responsibilities include:

• Managing the activities of the off-shift QA and QC teams to ensure production schedules are met within quality, safety, and operational standards.
• Leading inspection of all incoming components using customer standards, blueprints, certified test equipment, and ANSI/ASQC standards; supporting label inspection using SAP and scanning software.
• Providing guidance and resolving quality-related issues affecting production and product release.
• Participating in investigations related to quality deviations, out-of-specification materials, and non-conformances, and developing corrective actions.
• Assisting in internal quality audits and corrective actions to improve audit results.
• Facilitating documentation for new product start-ups and process transfers, ensuring completeness and readiness for production.

Additional duties:

• Assisting with safety investigations and corrective actions for hazards or incidents.
• Training, coaching, and developing employees to meet performance and departmental standards.
• Conducting performance reviews, managing budgets, and preparing SOPs and work instructions.
• Maintaining confidentiality of sensitive information.
• Supporting workplace demands, including working outside normal hours as needed.

Ideal candidate qualifications:

• Bachelor’s degree in Chemistry, Microbiology, Biology, or related science field.
• At least three years of supervisory or lead experience.
• Minimum of three years’ experience with laboratory equipment, aseptic sampling, and microbiological testing, preferably in cosmetics or pharmaceuticals.

We offer:

• Competitive salary with annual incentive
• Health, Vision, Dental, 401k
• Paid time off and holidays
• Opportunities for career advancement