8+ years of relevant experience, or 6 years with a Master's degree, or a PhD with 3 years' experience, or equivalent experience
Bachelor's or advanced degree in Computer Science, Computer Engineering, Electrical Engineering, or related technical discipline
Proficiency in .Net C# and full stack development practices
Experience with Agile methodologies and Test Driven Development (TDD)
Familiarity with Microsoft Azure DevOps and various web technologies like TypeScript and HTML5
Strong problem-solving skills and effective communication abilities
Medical device experience and knowledge of IEC 62304 is an advantage
Responsibilities
Develop and maintain software applications for neuromonitoring
Create and manage product software architecture
Oversee complete software development lifecycle as a key technical contributor
Document product software and maintain accurate project records
Collaborate with cross-functional teams to influence product development
Ensure compliance with regulations including FDA and ISO standards
Perform additional tasks as needed, including DevOps responsibilities
Benefits
Opportunity to work in a fast-paced, innovative environment
Engagement with a team committed to improving patient outcomes
Support for continuous professional growth and development
Participation in a culture valuing teamwork and accountability
Comprehensive support for maintaining compliance with industry standards
Full Job Description
Position Summary:
The Sr. Software Engineer position, Intraoperative Neuromonitoring, is responsible for the software applications & systems development function on software new product initiations and sustaining.
Essential Functions:
Develops and maintains software applications & systems development
Creates and maintains product software architecture
Takes the ownership of all aspects of software development as technical contributor
Writes product software documentation
Manages lifecycle for different projects inclusive of research, development, design, evaluation, testing and delivery to product management
Prioritizes work to identify the root cause and creates a corrective action plan that ensures timely resolution of issues
Follows software development standards and processes along with best practices for delivery of scalable and high-quality software
Works closely with cross functional engineers, developers and Product Management throughout organization to influence product development, assisting or improving products
Accountable for software development projects from beginning to finish
Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485
Performs other duties, as assigned, such as DevOps functions
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 upholds 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.
Qualifications:
Typically requires a minimum of 8 years of related experience with a Bachelor's degree, or 6 years and a Master's degree, or a PhD with 3 years' experience, or equivalent experience
Bachelor's or advanced degree in Computer Science, Computer Engineering, Electrical Engineering, or related technical discipline
Experience with Agile software development methodologies and TDD
Proficient understanding of software product design and development with object-oriented languages
Strong proficiency in .Net C# in a Windows and/or Web environment
Strong proficiency in Full stack development, .NET back end (C# preferred), JavaScript or TypeScript front end, HTML5, SCSS or CSS
Strong proficiency in Dependency injection/Inversion of Control
Git source control experience is a plus
Experience programming in C/C++
Experience with Azure DevOps is essential
Experience with LitElement or Webcomponents, SignalR/Websockets, Webpack, YAML and PowerShell is a plus
Experience in Qt is a plus
Excellent oral, written, and graphical communication skills
Medical device experience in a regulated industry is a plus. Familiar with IEC 62304
Strong problem-solving skills
Self-motivated and team player
Ability to travel up to 10% of the time
Physical Demands:
The physical demands listed here are representative of those that must be met by an 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
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
About Globus Medical
Globus Medical is a medical device company that develops and manufactures products for patients with musculoskeletal disorders. The company's products include spinal implants, surgical instruments, and orthopedic implants. Globus Medical was founded in 2003 and is headquartered in Audubon, Pennsylvania. The company has a strong focus on research and development and has received numerous awards for its innovative products. Globus Medical is committed to improving patient outcomes and has a strong reputation for providing high-quality products and services.
