Work Location: Providence County, RI

Summary:

Seeking a hands-on professional to oversee inspection and validation activities in a precision manufacturing setting. This role is ideal for individuals who excel in both production environments and structured quality systems, with a focus on continuous improvement and compliance with industry standards.

Responsibilities:

• Conduct mechanical and visual inspections of precision components using a range of metrology tools and equipment.
• Interpret engineering drawings, GD&T, and technical specifications to ensure product compliance.
• Support first article, in-process, and final inspections, maintaining accurate records and data integrity within the quality management system.
• Assist with process and equipment validations, including IQ/OQ/PQ protocols as required.
• Participate in nonconformance investigations, root cause analysis, and implementation of corrective and preventive actions (CAPA).
• Contribute to the preparation of documentation for customer submissions and regulatory requirements.
• Collaborate with cross-functional teams to drive process capability, stability, and continuous improvement initiatives.
• Support calibration activities and ensure measurement system integrity in alignment with quality standards.

Qualifications:

• Background in precision metal manufacturing (machining, grinding, tooling, or similar fields).
• Experience working within an ISO 13485 quality system is highly valued.
• Proficiency in dimensional inspection, metrology, process controls, and root cause analysis.
• Hands-on approach, comfortable working in both inspection labs and production floor environments.
• Strong PC skills, including Microsoft Word, Excel, and Outlook.
• Excellent written and verbal communication abilities.
• High attention to detail and a practical, problem-solving mindset.
• Experience with PPAP, validation protocols, NC/CAPA systems, SPC, and statistical tools is preferred.
• Familiarity with optical comparators, vision systems, and hand tools is advantageous.
• Prior experience in medical device manufacturing, aerospace, defense, or other regulated precision industries is a plus.

Published Category: Quality & Validation