Manufacturing Quality Assurance Inspector

DEKA Research & Development • Manchester, NH

3d • Onsite

About The Position

DEKA R&D has an immediate opening for a Manufacturing QA Inspector to work in a dynamic Medical Device Research, Development, and Manufacturing company. This position reports to the Manufacturing QA Manager and is a highly visible role with significant and direct impact on the manufacturing process and success of projects. About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

Requirements

• High School graduate or equivalent
• At least 3 years experience in a quality control role, medical device preferred
• Able to read and interpret technical documentation such as: Drawings, blueprints, operating procedures, ECOs, rework orders, etc...
• A basic understanding of proper handling of components sensitive to Electro-Static Discharge (ESD)
• Basic computer skills and technical knowledge; comfortable learning new software
• Familiar with AQL sample inspections
• Strong attention to detail
• Excellent communication skills, both verbal and written
• Self-motivated, Organized, and Excellent Prioritization skills

Responsibilities

• Perform in-process inspections of manufactured product according to device specifications and related documentation
• Support Engineering to ensure QMS compliance is met during all phases of research and development.
• Participate in the development and/or revision of Operation and Inspection Procedures
• Review Work Orders, Device History Records, and other documentation for compliance to established procedures, Good Documentation Practices (GDP), and the broader Quality Management System (QMS)
• General administration of the Nonconforming material process, including participation in Material Review Board meetings to facilitate disposition of rejected material, and use critical thinking to determine the best approach
• Review and provide feedback on proposed process changes when applicable to inspection activities, whether individually or in a cross-functional setting
• Perform audits against written procedures to help identify and recommend any necessary changes to the process
• Perform in-process inspection(s) in an ISO 14644 standard clean room

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED
• Number of Employees: 101-250 employees