Talent Software Services
Software Engineer III Job Summary: Talent Software Services is in search of a Software Engineer for a contract position in Gray, (near Portland, Maine), ME. The opportunity will be for one year with a strong chance for a long-term extension. Position Summary: We are seeking a professional to drive the integration and migration of in-house software tools used for functional testing in manufacturing. The ideal candidate will bring strong technical expertise in C# development, along with a solid understanding of medical device manufacturing processes and related software systems. This individual should be able to work independently and proactively, demonstrating ownership, problem-solving, and collaboration skills to ensure a smooth and efficient transition across multiple applications and cross-functional teams. Primary Responsibilities/Accountabilities: Review existing software tools for functional testing in manufacturing to determine compliance with Quality System requirements. Migrate software tools for functional testing from the existing manufacturing line in Irvine, CA to the new manufacturing site near Portland, ME. Work with manufacturing engineers to validate test equipment software and assist in identifying test strategies where necessary. Collaborate with cross-functional teams, including manufacturing engineers, systems engineers, quality, R&D, and PMO. Contribute to a culture of innovation, continuous improvement, and knowledge sharing within the R&D team. Qualifications: B.S or M.S. in Computer Science, Electrical Engineering, Computer Engineering, Software Engineering, or related major. Minimum 4 years of experience in software development or testing for medical device manufacturing. Engineering background with strong knowledge of manufacturing processes and systems. Familiarity in C# development, particularly for manufacturing-related applications. Familiarity with functional testing processes within manufacturing settings. Ability to collaborate cross-functionally with manufacturing, quality, and R&D teams. High ability to make knowledge-driven decisions and work with little supervision. Excellent documentation and communication skills for technical and process alignment. Strong problem-solving and analytical skills applied to production or testing workflows. Preferred: Experience working within or understanding manufacturing procedures and standards. Experience in active implantable medical devices. Proven ability to manage or execute software migration projects for in-house manufacturing software tools. Knowledge of ISO 13485 and FDA QSR. Working knowledge of IEC 60601 and/or 62304. If this job is a match for your background, we would be honoured to receive your application! Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let's talk!