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Globus Medical

Develops musculoskeletal implants and enabling technologies

Associate Project Engineer - Sustaining

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeAudubon, PA, USANo salary listedIn-person

About the Job

Requirements

  • A 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 computer-aided design software; Creo or SolidWorks is preferred.
  • 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 work in engineering and clinical environments, including operating rooms and cadaver labs.
  • Familiarity with risk management principles and design control processes in regulated industries.

Responsibilities

  • Design and implement product line extensions in collaboration with research and development, clinical, and regulatory teams.
  • Champion Design for Manufacturing 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 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 with cross-functional teams.
  • Lead and contribute to Post-Market Surveillance Reports and Periodic Safety Update Reports in compliance with global regulatory standards.
  • Drive risk analyses to assess and mitigate design and process risks.
  • Comply with the company Code of Conduct, the AdvaMed Code, the MedTech Code, other company policies, and applicable governmental laws, rules, and regulations in the United States and internationally; complete introductory and annual training and maintain knowledge of compliance as it applies to the role.
  • Represent the company professionally and uphold ethical business practices and socially responsible conduct in interactions with employees, customers, suppliers, and other third parties.

Desired 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.
  • Creo or SolidWorks experience.

About the Company

Globus Medical

Develops musculoskeletal implants and enabling technologies

Globus Medical makes medical devices for musculoskeletal problems, especially in spine, orthopedic, and neurosurgery. It has two segments: Musculoskeletal Solutions (implantable devices, biologics, and surgical instruments) and Enabling Technologies (imaging, navigation, and robotics for planning, guidance, and analysis). The products are sold to hospitals and clinics through a direct sales force and distributors, with revenue from device sales plus recurring disposables and services. The goal is to help patients recover from musculoskeletal issues by offering an integrated platform that combines implants with advanced guidance and analytics, while expanding its geographic reach.

Company size
1,001-5,000
Company stage
IPO
Headquarters
West Norriton Township, Pennsylvania
Founded
2003

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