Staff Electro-Mechanical Engineer

Position Summary.

The Staff Electro-Mechanical Engineer will support the development, manufacturing, and testing of Nuclein’s diagnostic medical devices. Working closely with the engineering and manufacturing teams, the individual will be responsible for executing various technical tasks, supporting instrument design work, troubleshooting equipment, route cause analysis of failure modes and documentation to support design changes.  

Essential Duties and Responsibilities. 

·         Collaborate with engineers and scientists to assemble, test, and troubleshoot diagnostic medical devices.

·         Support the engineering team in the design, implementation and documentation of experiments and product improvements.

·         Conduct testing and verification activities to ensure compliance with design specifications and regulatory requirements.

·         Assist in the setup and operation of test equipment, including data acquisition systems, measurement tools, and software.

·         Maintain accurate records of test results, observations, and equipment maintenance activities.

·         Assist in the development and optimization of manufacturing processes to improve efficiency and quality

·         Collaborate with cross-functional teams, including manufacturing, quality assurance, research and development, to address technical issues and implement solutions.

•                 Follow safety protocols and maintain a clean and organized work environment.

Education, Qualifications, and/or Experience. 

·         Bachelor’s degree in Electrical Engineering, Mechanical Engineering, or a related field.

·         2-3 years of experience building and troubleshooting instruments

·         Strong technical aptitude and hands-on experience with assembling and troubleshooting electronic and mechanical systems.

·         Familiarity with laboratory equipment, measurement tools, and data acquisition systems.

·         Proficiency in reading and interpreting technical drawings, schematics, and documentation.

·         Basic understanding of quality control principles and processes.

·         Excellent problem-solving skills and attention to detail.

·         Ability to work effectively in a fast-paced, collaborative team environment.

·         Strong organizational and time management skills to handle multiple tasks and priorities.

·         Good communication skills, both written and verbal.

·         Experience with medical device development or manufacturing is a plus.

•            Knowledge of regulatory requirements and quality management systems (ISO 13485, FDA QSR) is desirable.

Physical Requirements.  

·         Repetitive Motion: Some computer use

·         Weight Lifting: < 25 lbs.

·         Position: Time split between standing and sitting

·         Speaking and communicating

•            Occasional use of PPE may be required in laboratory/manufacturing/warehouse areas