Quality Supervisor - Manufacturing

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.

UFP Technologies, Inc. offers a competitive benefits package, including but not limited to:

• 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.

• 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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