Engineer III, Product Development

Location

Onsite

Full Time

• Bachelor's degree or higher in Mechanical Engineering, Biomedical Engineering, or related field from an accredited university
• A minimum of 4 years of product development experience; OR a master’s degree in a related field plus 2 years’ experience

• Experience in development and/or manufacturing of medical devices
• Experience with plastic injection-molded part design
• Proficiency in Solid Works
• Understanding of Geometric Dimensioning and Tolerancing (GD&T)

• Proficiency in mechanical design fundamentals, solid modeling, tolerance stack analysis, and design for manufacturing
• 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 behaviors and activities during times of change and handle unexpected situations with little to no guidance
• Exemplifies flexibility and resourcefulness; responds deftly to a variety of challenges and situations
• Ability to understand complexity, anticipate problems, and proactively diagnose
• Plan and carry out sequential projects
• Ability to analyze problems and troubleshoot solutions
• Apply solid cognitive ability to collecting, processing, and disseminating information
• Begin to demonstrate the ability to foster teamwork, collaboration, negotiation, and influencing others
• Engages colleagues with the Enable Values in mind
• Ability to maintain a positive attitude, show empathy for others, and always do the right thing
• Ability to understand your own emotions and their effects on your performance
• Ability to have a positive impact on others in support of company goals and a healthy work environment
• Excellent time management skills

• 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.
• 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, develop verification and validation strategies, and conduct risk management activities
• Support manufacturing process development
• Generate design history files following FDA and international standards
• Identify project risks and develop mitigation strategies