Full-Time

Quality Supervisor

Updated on 8/3/2026

Triangle Manufacturing

Triangle Manufacturing

51-200 employees

Medical device engineering and manufacturing partner

No salary listed

Upper Saddle River, NJ, USA

In Person

Category
Operations & Logistics (1)
Required Skills
FDA Regulations
Excel/Numbers/Sheets
Microsoft Outlook

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Requirements
  • A bachelor's degree from a four-year college or university and/or 3-5 years of related experience, or an equivalent combination of education and related experience in a regulated environment.
  • Ability to read, write, and speak English.
  • Knowledge of ISO and Food and Drug Administration regulations.
  • Well-developed supervisory, organizational, communication, and interpersonal skills.
  • Computer proficiency, including Microsoft Excel and Outlook.
  • Ability to work in and be challenged by a lean, team-based environment emphasizing accountability for customer service, quality, and Good Manufacturing Practice compliance.
  • Leadership skills, including the ability to plan, organize, coordinate, direct, and control the activities of the assigned group.
  • Willingness to be available to supervise multiple shifts and work occasional overtime as required.
  • Ability to read and interpret blueprints and understand how to inspect to blueprint specifications.
  • Ability to handle ambiguity in a fast-paced, performance-oriented environment.
  • Results-oriented approach.
Responsibilities
  • Supervise and lead a team of inspectors responsible for receiving, in-process, and final product inspection activities in compliance with quality standards, regulatory guidelines, and customer specifications.
  • Train and mentor inspection team members on quality standards, best practices, and regulatory requirements.
  • Work with production schedules to develop and implement inspection schedules and priorities, ensuring that inspection tasks are completed on time without compromising quality.
  • Monitor and report key performance indicators for inspection activities and implement improvements to optimize the inspection process.
  • Assist Engineering in investigating the root cause of customer or supplier rejections and internal quality failures, dispositioning non-conforming parts, and recommending and implementing corrective actions.
  • Perform in-process inspection audits, provide technical assistance to operators for inspection activities, and ensure compliance with good documentation practices.
  • Lead the team in identifying and implementing process improvements for inspection techniques and inspection technology.
  • Collaborate with Manufacturing, Engineering, Computer Numerical Control Programming, and Quality teams to address quality issues and ensure product quality throughout the manufacturing process.
  • Assist in developing, revising, and implementing Inspection Plans and Work Instructions.
  • Promote safety standards and address safety concerns in inspection areas to ensure a safe and compliant working environment.
  • Support continuous improvement initiatives and engineering projects throughout the organization.
  • Champion Lean manufacturing principles by encouraging lean thinking in development and production and conducting or coordinating training and implementation with managers and associates.
  • Directly supervise associates in one or more manufacturing areas in accordance with organizational policies and applicable laws.
Desired Qualifications
  • General understanding of computer numerical control machining and secondary operation processes.
  • Additional coursework in Business and Management.
  • Conflict management skills.
Triangle Manufacturing

Triangle Manufacturing

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Triangle Manufacturing provides engineering and manufacturing services for the medical device industry, guiding products from concept to market. It covers design, development, prototyping, pre-production, and volume production, with emphasis on powered instrumentation and complex assemblies. The company differentiates itself through tight tolerances, challenging components, early customer collaboration, and strict quality systems (FDA registered, ISO 13485:2003, ISO 9001:2008). Its goal is to help medical device companies bring ideas to market faster and more cost-effectively with integrated, high-quality engineering and manufacturing support.

Company Size

51-200

Company Stage

N/A

Total Funding

N/A

Headquarters

Upper Saddle River, New Jersey

Founded

1955

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Simplify Jobs

Simplify's Take

What believers are saying

  • Medical OEMs value Triangle's FDA registration and ISO 13485 quality systems.
  • Its design-for-manufacturability support can shorten development cycles and improve launch economics.
  • Long operating history supports relationship-driven outsourcing with orthopedic and surgical customers.

What critics are saying

  • Quality escapes or audit failures can stop regulated medical shipments and trigger customer loss.
  • Larger contract manufacturers outscale Triangle on bundled engineering, regulatory support, and pricing.
  • Dependence on OEM programs creates utilization risk if anchor customers re-source work.

What makes Triangle Manufacturing unique

  • Triangle specializes in medical and orthopedic product realization from concept through volume production.
  • It combines tight-tolerance machining, complex assemblies, and powered instrumentation expertise.
  • Four facilities and 107,000 square feet support engineering, prototyping, and scaled production.

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