Full-Time

Manufacturing

Triangle Manufacturing

Triangle Manufacturing

51-200 employees

Medical device engineering and manufacturing partner

No salary listed

Mahwah, NJ, USA

In Person

On-site in Upper Saddle River, New Jersey.

Category
Operations & Logistics (1)
Required Skills
Excel/Numbers/Sheets

Get referred to Triangle Manufacturing

See people who can refer or advise you

Requirements
  • 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 FDA regulations.
  • Well-developed supervisory, organizational, communication, and interpersonal skills.
  • Demonstrated computer proficiency, including Microsoft Excel and Outlook.
  • Demonstrated ability to work in and be challenged by a lean, team-based environment that places a high degree of emphasis on accountability for customer service, quality, and GMP compliance.
  • Demonstrated 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 occasional overtime as required.
  • Ability to read and interpret blueprints and understand how to inspect to the blueprint specifications.
Responsibilities
  • Supervise and lead a team of inspectors responsible for performing 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 all inspection tasks are completed on time without compromising quality.
  • Monitor and report key performance indicators (KPIs) for inspection activities and implement improvements to optimize the inspection process.
  • Assist Engineering to investigate the root cause of customer and/or supplier rejections and internal quality failures, disposition non-conforming parts, recommend and implement effective corrective actions as required.
  • Perform in-process inspection audits, provide appropriate technical assistance to operators for inspection activities, and ensure compliance with good documentation practices.
  • Lead the team to identify and implement process improvements on inspection techniques and inspection technology.
  • Collaborate with cross-functional teams including, but not limited to, Manufacturing, Engineering, CNC Programming, and Quality to address quality issues and ensure product quality throughout the manufacturing process.
  • Assist in the development, revision, and implementation of Inspection Plans, Work Instructions, etc.
  • Ensure a safe and compliant working environment by promoting safety standards and addressing safety concerns in the inspection areas.
  • Support continuous improvement initiatives and engineering projects throughout the organization.
  • Champion Lean manufacturing principles by encouraging lean thinking in all aspects of development and production, as well as conducting and/or coordinating training and implementation with managers and associates.
Desired Qualifications
  • General understanding of CNC machining and secondary operation processes.
  • Driven, results-oriented.
  • Ability to handle ambiguity in a fast-paced, performance-oriented environment.
  • Additional coursework in Business and Management.
  • Conflict management skills.
Triangle Manufacturing

Triangle Manufacturing

View

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

Get referred to Triangle Manufacturing

See people who can refer or advise you

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.

Help us improve and share your feedback! Did you find this helpful?