Engineer , Product Development

Qualifications

• Bachelor's degree or higher in Mechanical Engineering, Biomedical Engineering, or related field from an accredited university

• Training/proficiency in CAD software, especially Solid Works
• Understanding in mechanical design fundamentals and solid modeling.
• Proficiency utilizing the MS Office Suite (Project, Word, Excel, PowerPoint, Visio, Outlook).
• Strong analytical and creative problem-solving skills
• Excellent verbal communication and technical writing skills
• Ability to adapt to change and handle unexpected situations with close guidance
• Accepts direction on how to adapt approach to changing situations
• Ability to follow defined procedures
• Ability to stay focused on tasks, organize, compare, interpret basic data, and assess problems with guidance
• Work to acquire and develop new skills
• Ability to collaborate and maintain cooperative work relationships with others
• Engage colleagues with the Enable Values in mind
• Ability to maintain a positive attitude, show empathy for others, and always do the right thing

• Must be able to remain in a stationary position for extended periods of time
• Ability to constantly operate a computer and other office equipment, such as printer, telephone, etc.
• Ability to move about inside the office to access file cabinets, office machinery, etc.
• Ability to operate lab instrumentation and equipment
• Ability to lift and move 20 lbs
• Position requires being physically present on the premises during regular company hours or as approved by management

• Support the design and development of medical devices that adhere to company procedures, industry regulations and customer requirements
• Understand and follow the New Product Design process with a focus on quality
• Apply mechanical engineering principles and techniques to solve challenges related to product design, manufacturing, assembly, and testing
• Contribute to the development of product specifications, drawings, test protocols and reports.
• Convert user needs to input, supports the development of verification and validation strategies, and conducts risk management activities
• Generate design history files following FDA and international standards