Quality Control & Calibration Supervisor
Lincotek Group
Job Description
Location: Dayton, Ohio
\nDepartment: Quality
\nEmployment Type: Full-Time | Exempt
\n \nLead Quality. Drive Excellence. Make an Impact.
\n \nWe are seeking an experienced Quality Control & Calibration Supervisor to lead our QC team and play a key role in ensuring the quality, compliance, and timely release of products within a regulated medical manufacturing environment.
\n \nThis is an excellent opportunity for a hands-on quality professional who enjoys leading people, solving problems, working with precision measurement and metrology, and driving continuous improvement.
\nWhat You’ll Do
\n- \n
- Lead and supervise Quality Inspectors, Calibration personnel, and external inspection resources \n
- Coordinate daily QC activities and resources to support production priorities \n
- Review and approve Device History Records (DHRs), Certificates of Compliance (CoCs), and other product-release documentation \n
- Provide technical guidance on inspection methods, metrology, engineering drawings, and GD&T \n
- Oversee calibration activities and ensure measurement equipment meets established requirements \n
- Support investigations involving nonconforming products, root cause analysis, and corrective actions \n
- Utilize statistical quality tools, including SPC, MSA, and Gauge R&R \n
- Support internal, customer, vendor, ISO and FDA audits \n
- Ensure compliance with FDA Quality System Regulations (21 CFR Part 820), ISO 13485, and company quality procedures \n
- Coach, mentor, and develop QC team members while establishing strong performance standards \n
- Partner cross-functionally with Operations, Engineering, and other teams to continuously improve quality and efficiency \n
What We’re Looking For
\n- \n
- High School Diploma/GED required; Bachelor’s degree preferred \n
- 2+ years of relevant quality, inspection, metrology, or manufacturing experience \n
- Supervisory or team leadership experience preferred \n
- Strong knowledge of FDA Quality System Regulations, ISO 13485, and Good Documentation Practices \n
- Ability to interpret engineering drawings and GD&T \n
- Knowledge of metrology, calibration systems, and precision measurement equipment \n
- Experience with SPC, MSA, Gauge R&R, and statistical quality techniques \n
- Strong analytical, problem-solving, communication, and leadership skills \n
- Proficiency with Microsoft Office and quality-related software systems \n
Why Join Us?
\nThis is an opportunity to take a leadership role within a quality-driven medical manufacturing environment , where your expertise will directly contribute to product quality, regulatory compliance, operational excellence, and customer satisfaction.
\nIf you are a quality professional ready to lead a team, strengthen quality processes, and make a measurable impact , we’d love to hear from you.
\n \nApply today!
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