Sustaining Engineer

Globus Medical • San Antonio, TX

2d

About The Position

Bone Bank Allografts, a subsidiary of Globus Medical Inc., specializes in processing and distributing high-quality bone allografts for various medical procedures, including orthopedic, dental, and reconstructive surgeries. Our commitment to excellence, supported by Globus’ renowned engineering, drives our mission to advance patient care and medical innovation through precise and efficient allograft processing and distribution. Position Summary: The Sustaining Engineer will be responsible for engineering functions of existing product lines. This includes but is not limited to, continuous improvement ideation, design and development of line extensions, manufacturing improvements, post launch monitoring such as field failure evaluation, and market complication surveillance. This individual will work with field staff and all other functions of the company to ensure the high quality of all products continue throughout their lifecycles.

Requirements

• 1-3 years of design engineering experience preferably in the tissue engineering field
• Bachelor’s or master’s degree in a biomaterials or related biomedical field such as materials science and engineering, biomedical engineering, chemical engineering, tissue engineering, etc.
• Demonstrated self-starting skills
• Ability to manage multiple projects simultaneously and effectively within a fast-paced environment
• Well organized, detail oriented and team player capable of meeting deadlines
• Highly skilled in designing and executing experiments and will be a good lab steward

Nice To Haves

• Experience or familiarity with a cGMP environment, manufacturing human cells, biologics, biomaterials, or other product intended for human use is advantageous, but not required

Responsibilities

• Plan, design, and execute preclinical and laboratory studies to evaluate tissue-based biomaterials and systems.
• Analyze experimental and statistical data to generate technical reports and support data-driven strategic decisions.
• Lead Root Cause Analysis (RCA) investigations and implement Corrective and Preventive Actions (CAPA).
• Perform design verification and validation activities to ensure products meet defined specifications and regulatory requirements.
• Develop and maintain project documentation including SOPs, protocols, reports, batch records, Design History Files (DHF), and technical files.
• Maintain detailed project plans and ensure milestone adherence throughout the product lifecycle.
• Collaborate cross-functionally with manufacturing, quality, donor services, distribution, and supply chain teams to support product development and lifecycle management.
• Monitor post-launch product performance, collect field feedback, and implement continuous improvement initiatives.
• Track and trend performance data to identify system complications and drive process optimization.
• Ensure full compliance with internal quality systems and applicable regulatory standards (FDA, ISO, international regulatory bodies).
• Present technical findings, risk assessments, and project updates to cross-functional teams and leadership.
• Uphold company Code of Conduct and maintain compliance with AdvaMed Code, MedTech Code, and all applicable governmental regulations (U.S. and international).
• Represent the organization with professionalism, integrity, and commitment to ethical and socially responsible business practices.
• Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 1,001-5,000 employees