Senior Product Development Engineer - Knee Arthroplasty at Arthrex, Inc. in Naples, Florida

Job Description:

Requisition ID:	44378
Title:	Senior Product Development Engineer - Knee Arthroplasty
Division:	Arthrex, Inc. (US01)
Location:	INC- Naples FL (US08)

 

 

 

 

Main Objective: Responsible for full life cycle development of medical devices, which includes initiation, design, development, execution, and product maintenance.

 

Essential Duties and Responsibilities:

1. Designs components or functional systems, and modifies existing designs to develop or improve products and facilitate manufacturing operations.


2. Recommends alterations to development and design to improve quality of products and/or procedures.


3. Determines budgets and timelines for assigned projects.


4. Leads multifunctional new product project teams, as assigned by Engineering Manager, through project technical feasibility analysis, initiation, planning, execution, and termination, adhering closely to project timeline and budget. 


5. Maintains design history file for assigned projects, adhering to Arthrex design control procedures.


6. Provides Regulatory department technical support for assigned projects as needed.


7. Supports Marketing and Product Management with technical information to be used for training and marketing of assigned products.


8. Supports Manufacturing to provide processing improvements.


9. Supports surgeon and distributor customers by training and/or educating on technical aspects of assigned products as needed.


10. Determines necessity of testing and initiates testing of assigned products


11. Reports progress and status of assigned projects on a timely basis. 


12. May be required travel to attend trade shows and visit established accounts as well as prospective accounts. International travel may be required.

 

Education/ Experience

• 5 years of engineering experience in the commercialization of Arthroplasty devices


• 7 years of Orthopedic Medical Device engineering experience


• BS Degree Engineering required.  Mechanical, Biomedical, Electrical or Software Engineering preferred.  MS Preferred

 

Knowledge

Complete understanding and application of principles, concepts, practices, and standards.  Full knowledge of industry practices.

 

Skills

• Knowledgeable of FDA and ISO guidelines for the development of medical devices required.


• Manufacturing process knowledge preferred.


• Project management and communication skills training preferred.


• Working knowledge of anatomy from an orthopedic standpoint.


• Working knowledge of joint anatomy.


• Proficiency in designing products using a 3D-CAD program.  Pro/E and/or SolidWorks experience preferable.


• Technical knowledge in development methodologies, design, and project implementation.


• Knowledge of orthopedic surgery principles, theories, and products.


• Historical perspective on orthopedic surgery principals, theories, and products.

 

Reasoning Ability

Develops solutions to a variety of complex problems.  May refer to established precedents and policies.

 

Discretion/ Latitude

Work is performed under general direction.  Participates in determining objectives of assignment.  Plans schedules and arranges own activities in accomplishing objectives.  Work is reviewed upon completion for adequacy in meeting objectives.

 

 

 

 

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

 

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