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.
Experience or familiarity with a cGMP environment, manufacturing human cells, biologics, biomaterials, or other product intended for human use is advantageous, but not required
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
Physical Demands :
The physical demands listed here are representative of those that must be met by and employee to successfully perform the essential functions of this job.
Required to sit; climb or balance; and stoop, kneel, crouch or crawl
Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus.
Our Values :
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
Passionate about Innovation : Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate about our role in improving the lives of patients by continuously developing better solutions.
Customer Focused : We listen to our customers' needs and respond with a sense of urgency.
Teamwork : Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
Driven : We pursue our mission with energy and passion. We are nimble, results-oriented, and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.
Equal Employment Opportunity :
Globus Medical is an equal opportunity em
Benefits
Dental insuranceVision insurance
Additional Information
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.
Essential Functions:
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.
Globusmedical · San Antonio, TX