Electrical Engineer

Globus Medical•Audubon, PA

About The Position

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. Position Summary: We are seeking an engineer who is passionate about precision, obsessive about quality, and motivated by a mission to deliver breakthrough, evidence-based therapies that transform patient outcomes. If you aspire to lead innovation in implantable medical technology, this is your opportunity to make an impact.

Requirements

Bachelor’s degree in electrical engineering, or related field (Master’s preferred).
Minimum 7+ years of experience in electrical engineering. Equivalent years of experience may be substituted for the education requirement.
Strong understanding of analog/digital circuit design, embedded systems, and power electronics.
Proficiency in schematic capture and PCB layout tools (e.g., Altium Designer, OrCAD).
Familiarity with component lifecycle management and alternate part qualification.
Experience with V&V processes and regulatory documentation.
Excellent problem-solving, communication, and technical writing skills.
Working knowledge of FDA regulations, ISO standards, and QSR compliance.
Ability to manage multiple priorities and drive projects to completion in a cross-functional environment.

Nice To Haves

Experience in medical devices or other regulated industries (e.g., aerospace, automotive) is strongly preferred.

Responsibilities

Lead sustaining engineering efforts for existing neuromodulation products, ensuring continued compliance, reliability, and manufacturability.
Identify and manage EOL components, including sourcing and qualifying alternate parts.
Redesign electrical circuits and PCBs/PCBAs to accommodate component changes and improve performance or manufacturability.
Support verification and validation (V&V) activities for design changes, including test planning, execution, and documentation.
Collaborate with regulatory teams to support submission updates and ensure compliance with FDA, ISO, and QSR requirements.
Investigate field issues and manufacturing challenges, perform root cause analysis, and implement corrective actions.
Maintain design documentation, including schematics, BOMs, layout files, and change records in accordance with quality system procedures.
Interface with cross-functional teams, including R&D, Quality, Manufacturing, and Supply Chain, to ensure seamless implementation of changes.
Contribute to risk assessments and design reviews, ensuring robust and compliant design modifications.
Mentor junior engineers and provide technical leadership within the sustaining engineering team.
Support supplier communications and technical evaluations for alternate components and assemblies.
Travel up to 10%, including domestic and international visits to suppliers or manufacturing sites.
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
Ensures 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
Represents 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
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.