Quality Supervisor - Manufacturing

UFP Technologies•Providence, RI

3d•Onsite

About The Position

The Quality Supervisor leads the work-in-process quality control team and ensures that only material meeting product specifications leaves the Contech facility. The role oversees quality control testing, sampling, and control strategies; performs inspection and testing when needed; and recommends changes to inspection plans and test methods to improve inspection processes. The position is on-site full-time in Providence, Rhode Island, and requires residence within commuting distance (within 45 minutes). Applicants must be authorized to work for any U.S. employer; visa sponsorship is unavailable.

Requirements

Bachelor’s degree preferred, or equivalent work experience in a lead role.
Five or more years of QA/QC experience preferred.
Excellent communication skills and a track record of developing subordinates.
Strong analytical skills and attention to detail.
Ability to work independently with minimal direction.
Computer skills including Word, Excel, and ERP systems.
Ability to supervise and direct multiple employees in a fast-paced processing environment.
Strong verbal and written communication skills.
Ability to independently prioritize and manage multiple tasks.
Must be authorized to work for any employer in the United States; the company is unable to sponsor or assume sponsorship of an employment visa.
Must be within commuting distance of Providence, Rhode Island (within 45 minutes).

Nice To Haves

Experience in medical device manufacturing.
ASQ certification.

Responsibilities

Oversee quality control testing, sampling, and control strategies.
Perform inspection and testing when necessary.
Analyze product and process quality data to meet quality objectives.
Audit Quality Control staff for the quality and quantity of work performed.
Manage material release and final disposition activities.
Establish measurement systems analysis processes for people, processes, and products in the Quality Control Department.
Own process controls and the NCMR process.
Review and revise applicable QC documents and deviations.
Establish inspection requirements for new product projects.
Investigate customer complaints and corrective and preventive actions.
Assist with sales-related buyer visits when the Director of QA is unavailable.
Review records for thoroughness and accuracy.
Train QC staff and complete training records for the QC team.
Follow Contech’s Quality Management System, cGMPs, and ISO 13485 requirements.
Perform other duties as assigned or needed.