Principal Engineer

We are a leading global spine and orthopedics company with a premier portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions and a leading surgical navigation system. Our combined company is over 1,600 strong, with products distributed in 68 countries worldwide and a global R&D, commercial and manufacturing footprint, and this is just the beginning!

Come join our global team of dedicated professionals who through their extraordinary efforts demonstrate every day their commitment to our mission of improving the lives of patients. At SeaSpine and Orthofix our culture is built around Integrity and the core beliefs we live by: Exceed Expectations, Work Together, Be Respectful, Get Lean and Have Fun!

How you'll make a difference:

The Principal Engineer is responsible for partnering with franchise engineering leads to support technical efforts within and across Development franchises to bring highly technical medical device systems from concept through market introduction in accordance with FDA and ISO requirements. Furthermore, the Principal Engineer will provide field support for complex ongoing sustaining challenges on existing products. They will lead individuals / teams on project activities that include technical design and project team coordination to address a variety of highly complex technical problems that require specialized knowledge. The Principal Engineer will work with engineering management to assume technical responsibilities for all projects within or between various franchises, depending on the needs of the franchise.

The Principal Engineer may manage a team of Staff or other engineers focused on technical assistance and / or business development. Those engineers will either assist Principal Engineer on large, complex projects or manage projects of their own.

Your key responsibilities:

• Lead teams to develop and commercialize complex medical implant and instrument systems Establish project plans, develop product requirements, and coordinate other team activities in accordance with Design Control and Risk Management procedures
• Explore (confidential) Business Development ideas and ventures to vet integration opportunities
• Engage and lead business development activities, exploratory development, and various unbudgeted and unplanned proactive investigations
• Support franchise team Managers/Directors with their teams' technical requirements (Design consulting, DFM, manufacturing support, Design Reviews, Independent reviewers, etc.)
• Participate in, support, and supervise additional critical-to-business design projects through personnel management, dedicated project consulting within and across franchises, and technical mentorship
• Effectively interact with interdepartmental personnel and external partners to uphold project plans and achieve project objectives
• Generate complex implant and instrument CAD models and detailed engineering drawings using ProEngineer/Creo software to develop new device designs and/or maintain existing products
• Generate and analyze test data and reports to verify that designs meet functional and performance specifications
• Interface with vendors on technical issues while supervising designs throughout the manufacturing process
• Provide training, mentorship, and supervision to junior product development staff
• Proactively identify and correct recurring design issues across product development through education and training
• Assist with field sales support and training
• Develop intellectual property based on developed products
• Attend, participate in, and lead departmental meetings as scheduled
• Perform other duties as assigned

Who you are:

MINIMUM QUALIFICATIONS

• Bachelor's Degree in Engineering
• 12+ years' experience in medical devices (Spine/Orthopedic device preferred)
• Demonstrated ability leading teams and completing several projects on time and on budget with minimal supervision
• Expertise in FDA QSR and ISO 13485 principles, including Design Controls and Risk Management
• CAD experience required (Pro-Engineer/Creo, SolidWorks, or equiv.)
• Strong computer skills are required including proficient and accurate usage of CAD software (Pro-Engineer/Creo preferred), word processing (Word), spreadsheets (Excel), charting, flow charting, and graphs
• Ability to utilize a computer, telephone, fax, scanner, and copy machine as well as other general office equipment

PREFERRED QUALIFICATIONS

• Master's Degree in Engineering (Biomedical or Mechanical preferred)

The anticipated salary for this position for an employee who is located in California is $190,000 - $222,600 per year, plus bonus, and benefits.

We are committed to providing equal employment opportunities to all employees and applicants without regard to race (including traits historically associated with race, such as hair texture and protective hairstyles, including braids, locks, and twists), ethnicity, religion, color, sex (including childbirth, breast feeding, and related medical conditions), gender, gender identity or expression, sexual orientation, national origin, ancestry, citizenship status, uniform service member and veteran status, marital status, pregnancy, age, protected medical condition, genetic information, disability, or any other protected status in accordance with all applicable federal, state, and local laws.

This policy extends to all aspects of our employment practices including, but not limited to, recruiting, hiring, discipline, termination, promotions, transfers, compensation, benefits, training, leaves of absence, and other terms and conditions of employment.