Description • Manufacture medical products (capital equipment) by following documented procedures and Manufacturing instructions. • Perform equipment set-up and in-process testing to accomplish assigned task(s). • Develop manufacturing processes and work with engineers to create written procedures. • Support and train operators to manufacturing work instructions. • Assist in problem solving activities for design, process, and testing. • Assist in development and writing of test and measurement methods as needed. • Support in design and fabrication of fixturing for test and assembly. • Maintain accurate and legible manufacturing documentation. • Clearly communicate ideas and findings to supervisor and colleagues. Other duties as required. Requirements Minimum of three (3) years’ experience in medical device development. • Experience manufacturing medical device capital equipment. • Knowledge of Quality Systems. • Experience with Medical Device Regulation ISO 13485. • Experience working in a startup environment a plus. • Experience with electro-optics and opto-mechanical assemblies, laser and fiber optics components and processing a plus. • Willing to learn new technical skills and gain engineering knowledge. • Ability to handle small components and complex precision assemblies. • Ability to manage multiple objectives in a fast-paced environment. • Team player with good writing and communication skills. • Candidates must be able to work from both our Bedford and Sudbury locations and be willing to travel between sites as needed. EDUCATIONAL REQUIREMENTS: • 2-years technical degree or equivalent work experience.