New

Manufacturing Line Quality Engineer

Spectraforce Technologies
United States, Maine, Scarborough
Oct 10, 2026
Position Title: Manufacturing Line Quality Engineer Work Location: Scarborough, Maine, 04074 Work Arrangement: Onsite Duration: 3-month assignment Work Schedule: Rotating 3rd Shift C Flight: Sunday-Tuesday, plus alternating Wednesdays Hours: 6:00 PM-6:00 AM D Flight: Thursday-Saturday, plus alternating Wednesdays Hours: 6:00 PM-6:00 AM Important: Candidates must be generally available to work either the C Flight or D Flight. Position Summary Our organization is part of The Organization's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. The position of Manufacturing Line Quality Engineer is within our Infectious Disease business unit located at all sites under The Organization Diagnostics Scarborough QMS. In this role you will provide support for product quality assurance, process improvements, and all quality system programs. Background & Context This job description will be reviewed periodically and is subject to change by management. Key Responsibilities Support production with resolution of quality issues in accordance with established procedures. Support production on the manufacturing floor, ensuring adherence to procedures and ensure appropriate device history record (DHR) documentation. Supports line clearances, reworks, and inspections as required. Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies. Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices. Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities. Other duties as assigned, according to the changing needs of the business. Qualification & Experience Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life Science or other technical field or the equivalent combination of education and experience. Working knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software. Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements Strong technical writing skills and effective communication skills Additional Information An equal opportunity employer, The Organization welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities.