Quality Control Supervisor

Ace Sanitary; Olde West Chester (OH); On-site; USD 70,000 - 100,000; Full time

Job summary

Ace Sanitary is seeking a hands-on Quality Control Supervisor to lead the inspection team on the manufacturing floor, coach staff, and drive process improvements. You’ll ensure incoming components and finished products meet quality standards and regulatory requirements while balancing day-to-day priorities with long-term capability building.

Successful candidates will have extensive quality experience in regulated environments, demonstrable leadership, and strong analytical skills to translate

Qualifications

• Associate degree or equivalent; bachelor’s degree preferred.
• 6+ years of Quality experience in medical devices or regulated manufacturing.
• 2+ years supervisory experience and 2+ years regulatory/compliance experience.
• Auditing certification or relevant auditing experience.
• Working knowledge of ISO 9001 and ISO 13485; 3-A Sanitary Standards and ISO 14644 experience are a plus.
• Experience with quality tools such as SPC, CAPA, Root Cause Analysis, QMS, Metrology, Gage R&R, Control Plans, AQL/Batch Sampling, MSA, Lean Manufacturing, NPI, and 5S/Kaizen.

Responsibilities

• Lead daily inspection activities across Production, balancing workload and priorities to support on-time inspection and CoC release.
• Coach, develop, and hold Quality Control team members accountable for performance, quality, and training requirements.
• Oversee incoming and finished-goods inspections, sampling plans, test procedures, and First Article Inspections (FAI).
• Manage nonconforming material and support MRB/RMA activities.
• Track key metrics including inspection cycle time, backlog, throughput, and defect rates, and take action when targets are not met.
• Provide technical guidance on SPC, Control Plans, metrology, inspection methods, and measurement systems.
• Lead continuous improvement efforts using root cause analysis, CAPA, and structured problem-solving.
• Support internal and external audits and corrective actions.
• Partner with Quality, Production, Engineering, HR, and other teams to meet customer and business needs.
• Champion a culture of safety, quality, integrity, teamwork, and continuous improvement.

Skills

Quality leadership

Regulatory compliance

Problem-solving

Communication

Team building

Education

Associate degree or equivalent

Bachelor’s degree preferred

Tools

GD&T understanding

ERP systems

Power BI

Job description

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.

Description

Quality Control Supervisor

Lead Quality. Develop People. Drive Improvement.

We’re looking for an experienced Quality Control Supervisor who enjoys being close to the manufacturing floor, developing people, solving problems, and making processes better.

In this role, you’ll lead our Quality Control inspection team and help ensure that incoming components and finished products meet our quality standards, customer requirements, and applicable regulatory expectations. You’ll balance day‑time inspection priorities with the bigger picture - building team capability, improving processes, reducing bottlenecks, and strengthening a culture of quality and continuous improvement.

If you’re a hands‑on quality leader who can coach a team, interpret technical requirements, and turn quality data into action, we’d like to hear from you.

What You’ll Do

• Lead daily inspection activities across Production, balancing workload and priorities to support on‑time inspection and Certificate of Conformance (CoC) release.
• Coach, develop, and hold Quality Control team members accountable for performance, quality, and training requirements.
• Oversee incoming and finished‑goods inspections, sampling plans, test procedures, and First Article Inspections (FAI).
• Manage nonconforming material and support MRB/RMA activities.
• Track key metrics including inspection cycle time, backlog, throughput, and defect rates, and take action when targets are not met.
• Provide technical guidance on SPC, Control Plans, metrology, inspection methods, and measurement systems.
• Lead continuous improvement efforts using root cause analysis, CAPA, and structured problem‑solving.
• Support internal and external audits and corrective actions.
• Partner with Quality, Production, Engineering, HR, and other teams to meet customer and business needs.
• Champion a culture of safety, quality, integrity, teamwork, and continuous improvement.

What You Bring

• Associate degree or equivalent experience; bachelor’s degree preferred.
• 6+ years of Quality experience in medical devices or another regulated manufacturing environment.
• 2+ years of supervisory/team leadership experience and 2+ years of regulatory/compliance experience.
• Internal/external auditing certification or relevant auditing experience.
• Working knowledge of ISO 9001 and ISO 13485; 3-A Sanitary Standards and ISO 14644 experience are a plus.
• Experience with quality tools and methods such as SPC, CAPA, Root Cause Analysis, QMS, Metrology, Gage R&R, Control Plans, AQL/Batch Sampling, MSA, Lean Manufacturing, NPI, and 5S/Kaizen.
• Ability to interpret customer drawings, specifications, and GD&T.
• Strong leadership, communication, organization, and problem‑solving skills.
• Proficiency with ERP systems and Microsoft Office; Power BI experience is a plus.

What Success Looks Like

• You’ll build an engaged and accountable team, improve inspection performance and productivity, strengthen collaboration across departments, and drive sustainable improvements in quality and manufacturing processes.
• Our culture is grounded in Integrity & Trust, Creativity & Courage, Teamwork, and Excellence. We value leaders who communicate openly, listen respectfully, support their teams, and lead by example.

Additional Requirements

• This is a hands‑on manufacturing role requiring regular time on the production floor. Candidates must be able to stand and walk for extended periods, safely navigate a manufacturing environment, frequently lift up to 25 lbs. and occasionally lift up to 50 lbs.
• Some overtime may be required, including occasional Saturdays.

Attendance Requirements: Attendance on a regular, consistent basis is mandatory.

Accommodations: If you need reasonable accommodation under the ADA or other state or federal law to perform the essential job functions as listed above, you may request accommodation in the interview process or list it below:

Position Requirements

Full-Time/Part-Time Full-Time

Shift First

Position Quality Control Supervisor

Division Ace Sanitary

Exempt/Non-Exempt Exempt

Location Ace Sanitary Holdings

This position is currently accepting applications.