• 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. 

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.