Engineer Level II

Responsibilities:

• Act independently with minimal supervision to conduct smaller approved projects. Expected to make suggestion on improvements based on recent technical knowledge.
• Able to contribute to cost estimating of major capital budget items and the spending of approved project funds.
• Contribute to the planning and execution of components of the development process, which apply to product revision or enhancement or a defined piece of a larger project.
• Ability to manage routine small projects without assistance.
• Investigate and analyze design improvement suggestions. Recommend design improvements.
• Perform standard engineering assignments which are typically a significant portion of a larger project. Select sound techniques to solve problems and make design recommendations under direction of supervisor. Assess results for application, validity and conformance to specifications. Recommend material and process specifications.
• Utilize engineering tools to solve straightforward problems (e.g., FMEA, Finite Element Analysis, Process Modeling, Design of Experiments, Mold Flow, SPC)

Qualifications:

• BS in Engineering (Mechanical, Chemical, Bioengineering, or Biomedical), MS preferred
• 1-3 years of medical device product development experience
• Statistical background helpful
• Knowledge of DHF or DHF Remediation
• Medical Device Product Life Cycle, Design Controls
• Software: Microsoft Office: Word, Excel (pivot tables, V-looks), Outlook, PowerPoint; Minitab; DOORS; CAD

Skills:

• Team Player
• Good Communicator
• Reliable