Quality Engineer

Why Join Us? Join a team shaping life-saving medical technologies while accelerating your career in a high-growth global environment. At Viant, you'll help bring innovative healthcare solutions to patients worldwide while growing in a collaborative, people-first culture. Guided by our promise, We're In It For Life, we invest in your development, well-being, and ability to make a meaningful impact every day. About the Company Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. About the Site Located in Brimfield, Massachusetts, our facility specializes in precision manufacturing for the medical device industry. Team members work in a collaborative environment focused on quality, innovation, and continuous improvement. The site offers opportunities to work closely with manufacturing, engineering, quality, and supply chain teams to deliver products that improve patient lives worldwide. New employees are eligible for the following benefits effective date of hire! Full Medical, Dental & Vision, 401(k), effective on your 1st day Generous paid time off benefits and 10 paid Holidays Growth Opportunities On-Demand Pay: Access your pay as soon as you have earned it! We offer market competitive compensation. Potential salary range for this role is $70,000-95,000 annual wage. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. Responsibilities Adheres to Viant Core Beliefs and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory requirements. Supports regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality. Monitors manufacturing of assigned products, assuring compliance with DMR while providing deviation/waiver guidance and assuring complete and correct Device History Records are maintained. Leads and implements various product and process improvement methodologies. Review the adequacy and correctness of changes to Bill of Materials (BOM’s), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc. Leads in the completion and maintenance of risk analysis. Leads generation and completion of protocols and reports for test method validations. Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable. Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures. Ensures that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence. Effectively communicate and interact with customers. Leads and manage complaint investigations. Acts as a lead in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis. Assists with product transfers. Works with suppliers…

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