Primary Duties:

　　Assists in the definition, proof of concept, development, implementation and/or support of technical or business solutions by performing specific tasks within the scope of the assigned activity.

　　Identifies issues and uses problem-solving tools to formulate the necessary activities to provide successful solutions.

　　Ensures quality of deliverables by following the appropriate design practices and departmental procedures for design control and regulatory compliance.

　　Creates appropriate documentation such as technical communications, reports, meeting notes and other relevant technical documentation within the role’s function.

　　Prioritizes activities within the scope of the assignments to ensure schedules or quality of work is successfully achieved.

　　Ability to define, review and check product Bill of Materials (BOM) structures, assembly instructions and test procedures.

　　Works with internal department and project specific teams.

　　Training and Education:

　　Requires Bachelor’s Degree in Mechanical Engineering with 3+ years of engineering experience or Master’s Degree in Mechanical Engineering with 1+ year of engineering experience. Medical Device field is preferred.

　　Knowledge & Experience:

　　Knowledge of electro/mechanical production processes.

　　Technical skills in the relevant Manufacturing Engineering disciplines

　　Knowledge of FDA, QSR and ISO quality systems.

　　Timeliness and quality of technical development activities.

　　Quality and completeness of documentation.

　　Development of personal autonomy and time management skills.

　　Ability to handle multiple assignments and tasks.

　　Knowledge of CAD systems (Solidworks, CREO, Unigraphix)