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Carlsbad, California, United States
Onsite
Why Orthofix?
Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech.
Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.
JOB PURPOSE
The Senior Design Engineer is responsible for assisting in the development of new medical device systems from concept to market introduction in accordance with FDA and ISO requirements. The Senior Design Engineer will also collaborate with other engineers to provide solutions to a variety of technical problems under immediate supervision from senior engineering staff.
Execute on a range of responsibilities within the Product Development team, ranging from individual instrument and implant design and development to leadership of projects.
Support and assist with project-critical responsibilities from direct management or senior engineering peers while operating independently for many of their direct responsibilities.
Generate implant and instrument CAD models and detailed engineering drawings using ProEngineer/Creo software to modify/sustain existing products and support new device designs.
Generate documentation to support designs in accordance with Design Control and Risk Management procedures.
Generate and analyze test data and reports to verify that designs meet functional and performance specifications.
Effectively interact with external and internal personnel to establish necessary design inputs, uphold project plans, and achieve project objectives.
Interface with vendors on technical issues while supervising designs throughout the manufacturing process.
Collaborate with cross-functional teams to address product complaints, manufacturing challenges, nonconforming material reports (NCMRs), and related issues.
Perform other related duties as assigned.
MINIMUM QUALIFICATIONS
The requirements listed below are representative of the education, knowledge, skill and/or ability required for this position.
Education/Certifications:
Bachelor’s Degree in Engineering or similar field of study
Experience, Skills, Knowledge and/or Abilities:
2-5 years’ experience in medical device field
CAD experience required (Pro-Engineer/Creo, SolidWorks, nTopoglogy 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
The education, knowledge, skills and/or abilities listed below are preferred qualifications in addition to the minimum qualifications stated above.
Education/Certifications:
Master’s Degree in Engineering (Biomedical or Mechanical preferred)
Additional Experience, Skills, Knowledge and/or Abilities:
Additive Manufacturing / Metal 3D Printing experience
nTopology experience
Medical device experience
PHYSICAL REQUIREMENTS / ADVERSE WORKING CONDITIONS
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities, skills, and/or demands required of the position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to allow qualified individuals with a disability to perform the essential functions and responsibilities of the position.
No additional physical requirements or essential functions for this position.
The anticipated salary for this position for an employee who is located in California is $91,000 to $110,000 per year, plus bonus, and benefits.
DISCLAIMER
The duties listed above are intended only as representation of the essential functions of this position. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. The job description does not constitute an employment agreement between the employer and employee and is subject to change at the sole discretion of the employer. Nothing in this document alters an employee’s at-will employment status.
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, religious creed (including religious dress and grooming practices), color, caste, 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 (40 and over), protected medical condition (including cancer and genetic conditions), genetic information, disability (mental and physical), reproductive health decision-making, medical leave or other types of protected leave (requesting or approved for leave under the Family and Medical Leave Act or the California Family Rights Act), domestic violence victim status, political affiliation, 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.