Description

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.

How you'll make a difference?

This position is responsible for providing Design Assurance support to product development activities, selected sustaining, and specials projects within Orthofix. The position must also ensure compliance with applicable product standards, governing laws and regulations, and company quality system requirements.

What will your duties and responsibilities be?

The following are the essential functions of this position. This position may be responsible for performing additional duties and tasks as needed and assigned.

• Participate as a product development cross-functional core team member

• Ensure project design controls requirements are being met

• Educate and guide product development team on quality and design controls best practices

• Collaborate with multiple disciplines to ensure completion of project objectives

• Risk management and hazard analysis

• Reliability and failure analysis, FMEAs

• Design validation plan and protocol development

• Evaluate design changes for impact to standards and product essential performance

• Establish acceptance criteria and ensuring compliance with technical standards

• Biocompatibility and Sterilization

• Review specifications to ensure appropriate dimensioning and tolerances

• Input to process development and design for manufacturing

• Input to and approval of process validation activities

• Measurement System Analysis

• Input to, and development of, specifications, standards, test protocols, test reports, procedures and other documentation and records related to design and development

• CAPA/NCMR investigations

What skills and experience will you need?

The requirements listed below are representative of the education, knowledge, skill and/or ability required for this position.

Education/Certifications:

• Bachelor's degree in mechanical or electrical engineering

Experience, Skills, Knowledge and/or Abilities:

• 3-5 years of relevant experience

• Root cause analysis, problem solving, continuous improvement

• Excellent technical writing skill and ability to communicate well (both written and verbal) laterally and vertically

• Excellent time management and ability to balance multiple deliverables simultaneously

• Logical cognitive skills and ability to apply scientific methods

• Ability to identify variables affecting quality

• Ability to meet deadlines and/or objectives as directed

What qualifications are preferred?

The education, knowledge, skills and/or abilities listed below are preferred qualifications in addition to the minimum qualifications stated above.

Education/Certifications:

• ASQ Certified Quality Engineer (CQE)

• Master's degree in engineering

Additional Experience, Skills, Knowledge and/or Abilities:

• Software design, IEC 62304, cybersecurity

• Worked with Spinal or Orthopedic medical devices

• Medical device or other health-related field experience

• CAD

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.

• This position requires frequent light lifting of up to 15lbs.

• This position requires frequent repetitive motion involving substantial movements of the wrist, hands and/or fingers; or grasping with hands and/or fingers.

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.

Since 1980, Orthofix has evolved and grown to become one of the leading medical device companies with a spine and orthopedics focus in the world. Our newly merged Orthofix-SeaSpine organization is a leading global spine and orthopedics company with a comprehensive portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions, and a leading surgical navigation system. Our products are distributed in 68 countries worldwide.

Our medical device company is headquartered in Lewisville, Texas, and has primary offices in Carlsbad, CA, and Verona, Italy. Our combined company's global R&D, commercial and manufacturing footprint also includes facilities and offices in Irvine, CA; Toronto, Canada; Sunnyvale, CA; Wayne, PA; Olive Branch, MS; Maidenhead, UK; Munich, Germany; Paris, France; and São Paulo, Brazil.

Founded in Verona, Italy, and now headquartered in Lewisville, Texas, Orthofix is proud to be recognized as the 8th Largest Orthopedic Medical Device Company in the World by Medical Design & Outsourcing magazine. Orthofix is committed to improving patients' lives and delivering innovative, quality-driven solutions that empower physicians and healthcare organizations to meet the needs of their patients every day.

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