Quality Supervisor – Manufacturing

Dielectrics, a UFP Technologies company

Providence (RI)

On-site

USD 65,000 - 95,000

Full time

32 hours ago
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Benefits offered by this job

Health benefits
401K with match
Paid time off
Employee discounts

Job summary

Contech Medical, a UFP Technologies company, seeks a Quality Supervisor to lead the on-site QA/QC team in Providence, RI. You will ensure only material meeting specifications leaves the facility and drive improvements to inspection plans.

You will supervise testing, analyze data, manage documentation, and ensure adherence to cGMP and ISO 13485. Strong communication and leadership are essential to develop and coach staff.

Qualifications

  • Bachelor’s degree or equivalent work experience in a lead QA/QC role.
  • 5+ years’ experience in QA/QC preferred, medical device manufacturing a plus.
  • ASQ certification is preferred.
  • Excellent communication skills and a track record of developing subordinates.
  • Strong analytical skills with detail orientation and ability to work independently.

Responsibilities

  • Oversees quality control testing, sampling, and control strategies.
  • Performs inspection and testing when necessary.
  • Analyzes product and process quality data to meet quality objectives.
  • Audits QC staff for quality and quantity of work performed.
  • Manages material release and final disposition activities.
  • Establishes measurement systems analysis processes for QC.

Skills

Communication
Analytical thinking
Detail orientation
Independent work
Supervisory ability

Education

Bachelor’s degree
ASQ certification

Tools

Word
Excel
ERP systems

Job description

Quality Supervisor - Manufacturing

I/L GeneralFull-Time Quality Assurance
Providence, RI, US

About Contech

Contech Medical, a UFP Technologies company, is a global leader in the design, development, and manufacture of class III medical device packaging primarily for catheters and guidewires. Our experience in packaging, assembly and distribution encompasses multiple continents and the largest medical device companies in the world.

Benefits
  • Medical, Dental, Vision, Life, Disability Insurance
  • 401K with a matching contribution
  • Paid time off, Paid holidays, Employee discounts and much more!
Location

This position is on-site full-time in Providence, RI. The position holder will need to be within commuting distance (within 45 min).

Applicants must be authorized to work for any employer in the U.S. At this time, we are unable to sponsor or assume sponsorship of an employment visa.

Summary

The Quality Supervisor effectively leads the work-in-process quality control team, ensuring only material conforming to product specifications leaves Contech facility. The role recommends changes to inspection plans and test methods to improve inspection processes.

Duties And Responsibilities
  • Oversees quality control testing, sampling, and control strategies.
  • Fills in and performs inspection and testing when necessary.
  • Analyzes product and process quality data to meet quality objectives.
  • Audits Quality Control staff workforce for quality and quantity of work performed.
  • Manages material release and final disposition activities.
  • Establishes measurement systems analysis processes, related to people, processes, and products for the Quality Control Department.
  • Acts as the owner for process controls and NCMR process.
  • Reviews and revises applicable QC documents, deviations, etc.
  • Establishes inspection requirements for new product projects.
  • Investigation of customer complaints/corrective and preventive actions.
  • Assists with sales-related buyer visits when the Director of QA is unavailable.
  • Reviews records for thoroughness and accuracy.
  • Trains QC and complete training records for QC team.
  • Responsible for following Contech’s Quality Management System, cGMP’s, and ISO 13485 requirements.
  • Performs all other duties as assigned or needed.
Qualification Requirements
  • Bachelor’s degree preferred or equivalent work experience in a lead role.
  • 5+ years’ experience in QA/QC preferred.
  • Experience in medical device manufacturing a plus.
  • ASQ certification is preferred.
  • Excellent communication skills and a track record of developing subordinates.
  • Strong analytical skills. Detail oriented. Able to work independently with minimal direction.
  • Computer skills to include Word, Excel, and ERP systems.
  • Must be able to supervise and direct multiple employees in a fast-paced, processing environment.
  • High level of communication skills, both verbal and written.
  • Ability to independently prioritize and manage multiple tasks.

Contech, a UFP Technologies company, is an Equal Opportunity employer Minorities/Women/Veterans/Disabled.

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