Associate Project Engineer, Sustaining at Globus Medical in Audubon, PA

Job description

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible. The Associated Project Engineer - Sustaining in Product Development team plays a pivotal role in supporting the ongoing success and optimization of our commercial product portfolio. This position bridges engineering, quality, clinical, and manufacturing functions to ensure that products on the market perform to the highest standards of safety, usability, and efficiency. You will contribute to sustaining engineering efforts, evaluate field performance, and implement improvements that directly impact patient outcomes. Key Responsibilities Design and implement product line extensions , working closely with the R&D, clinical, and regulatory teams. Champion Design for Manufacturing (DFM) improvements across launched product lines to optimize cost, reliability, and manufacturability. Resolve manufacturing challenges through vendor coordination and iterative design updates . Provide technical support during cadaver labs and customer engagement meetings to validate and refine device performance. Support surgical cases in the operating room , working directly with surgeons to gather real-time feedback and identify clinical opportunities for improvement. Perform product scrap analysis and coordinate remediation strategies to improve yield and performance. Conduct complaint evaluations , identify root causes, and implement corrective actions in collaboration with cross-functional teams. Lead and contribute to Post-Market Surveillance Reports (PMSR) and Periodic Safety Update Reports (PSUR) in compliance with global regulatory standards. Drive risk analyses to assess and mitigate design and process risks. Adhering to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies. Ensure Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role Representing the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties of Globus Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Required Qualifications Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related field. 0-2 years of experience in product development or sustaining engineering within the medical device industry. Proficiency with CAD software (CREO or SolidWorks preferred) for mechanical design and documentation. Proficiency with Microsoft Excel, PowerPoint, and Project for data analysis, presentations, and project tracking. Strong analytical and problem-solving skills with attention to detail. Effective verbal and written communication skills for cross-functional collaboration. Ability to thrive in both engineering and clinical environments, including operating rooms and cadaver labs. Familiarity with risk management principles and design control processes in regulated industries. Preferred Qualifications Internship or co-op experience in a regulated industry, ideally medical devices. Exposure to post-market surveillance activities or complaint handling systems. Understanding of ISO 13485, FDA 21 CFR Part 820, or EU MDR regulations. Our Values : Our Life Moves Us philosophy is built on four value