Engineer II, Orthopedic Product Development

Arthrex, Inc.; Naples (FL); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

401(k) Matching

Annual Bonus

Wellness Program

Onsite Medical Clinics

Onsite Lunch

Tuition Reimbursement

Paid Time Off

EAP

Job summary

Arthrex, Inc. is a global medical device company seeking an Engineer II - Product Development to support the Upper Extremity team.

You will lead the full lifecycle development of orthopedic devices, focusing on suture-based solutions, plating systems, implants and instrumentation, with emphasis on Shoulder and Biceps initiatives. The role requires problem-solving, understanding of product development and quality systems, and exposure to regulatory submissions.

Qualifications

• Bachelors degree in Engineering required.
• 2 years of relevant work experience outside of academic coursework or internships required.
• Experience with medical devices and regulatory submissions helpful.

Responsibilities

• Design components or systems and modify existing designs to improve products and manufacturing operations.
• Lead cross-functional project teams through feasibility, initiation, planning, execution and termination.
• Maintain design history files and provide regulatory support as needed.
• Support Marketing and Product Management with technical information for training and marketing.
• Travel to trade shows and accounts as required.

Skills

Project management

Communication

Anatomy knowledge (ortho)

FDA/ISO guidelines

Manufacturing processes

Education

Bachelor's degree in Engineering

Job description

Arthrex, Inc. is a global medical device company seeking an Engineer II - Product Development to support the Upper Extremity team.

You will lead the full lifecycle development of orthopedic devices, focusing on suture-based solutions, plating systems, implants and instrumentation, with emphasis on Shoulder and Biceps initiatives. The role requires problem-solving, understanding of product development and quality systems, and exposure to regulatory submissions.