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Quality Control Supervisor

LocationPhiladelphia, Pennsylvania, United States
TypeOnsite

Precision Manufacturing | Medical Device | Aerospace | Philadelphia, PA


We are seeking a Quality Control Supervisor to lead day-to-day inspection activities in a regulated, high-precision manufacturing environment. This is a hands-on supervisory role responsible for ensuring inspection accuracy, procedural compliance, and timely execution of Quality Control activities while supporting production and customer requirements.The ideal candidate brings strong technical inspection expertise, working knowledge of FDA/ISO environments, and early leadership experience within precision manufacturing.

Key Responsibilities


  • Supervise daily Quality Control inspection activities, including first article, in-process, and final inspections
  • Perform inspections as needed to maintain throughput and address complex measurement requirements
  • Interpret engineering drawings and apply GD&T to inspect small, precision-machined components
  • Ensure compliance with established quality procedures, FDA regulations, and ISO 13485 requirements
  • Assign inspection work, set daily priorities, and monitor inspection queues
  • Identify, document, and control nonconforming material; support MRB activities with accurate data
  • Communicate inspection results and quality concerns to Quality Engineering, Manufacturing, and leadership
  • Support customer and regulatory audits by providing inspection records and floor-level assistance
  • Train, coach, and mentor Quality Inspectors on inspection methods and documentation practices
  • Promote a culture of accountability, consistency, and attention to detail within the QC team

Qualifications


  • 6–8 years of Quality Control or inspection experience in a regulated manufacturing environment(medical device, aerospace, or similar)
  • 1–3 years of lead or supervisory experience preferred
  • Strong working knowledge of GD&T, inspection methods, and sampling techniques
  • Experience inspecting small, precision-machined parts
  • Working knowledge of FDA 21 CFR Part 820 and ISO 13485
  • Strong organizational, communication, and interpersonal skills
  • Proficiency with Microsoft Word, Excel, and quality documentation systems
  • ASQ Certified Quality Inspector (CQI) or equivalent certification preferred

Compensation


  • Base Salary: Up to $90,000 per year
  • Bonus eligibility and benefits package included
  • Compensation is commensurate with experience and technical skill level

Why Join Us


You’ll play an important role in ensuring product quality and regulatory compliance in a precision manufacturing environment while working closely with engineering, manufacturing, and quality leadership. This role offers hands-on impact, professional growth, and exposure to regulated industries.

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