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