V

Varian

Tech-enabled radiation oncology hardware and software

Senior Compliance Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeGeorgia, USA

About the Job

Requirements

  • Solid hands-on experience with medical device compliance testing and engineering is required.
  • Strong working knowledge of standards applicable to complex active medical devices, including IEC 60601-1 with applicable collateral and particular standards, IEC 60601-1-2 for electromagnetic compatibility, ISO 14971, ISO 13485, FDA 21 CFR 820, IEC 62304, and, for sterile single-use consumables, ISO 10993 and applicable sterilization standards.
  • Demonstrated experience working with external compliance and test laboratories, such as TÜV or equivalent, to test medical devices is required.
  • Experience interpreting standards and translating clauses into system-specific design and verification requirements is required.
  • Experience with design reviews and design control procedures is required.
  • Strong documentation and communication skills are required.
  • At least 8 years of medical device compliance and product safety engineering experience is required.
  • A bachelor's degree in Electrical, Mechanical, Biomedical, or Systems Engineering, or a closely related field, is required.
  • Willingness to travel up to 20% is required.

Responsibilities

  • Lead compliance engineering and product safety strategy for EVR across the Monadnock program and other product development efforts.
  • Identify applicable standards, interpret individual clauses in the context of the system, and derive clear, system-specific product safety and compliance requirements for design teams.
  • Partner with mechanical, electrical, consumables, and software design engineers from requirements development and early design through design review and compliance verification.
  • Plan, coordinate, and manage compliance testing with external verification laboratories, and own relationships with those laboratories for electromagnetic compatibility, electrical safety, and other product safety testing.
  • Participate in design reviews in a compliance capacity to ensure the design meets compliance requirements.
  • Lead compliance verification planning and execution, and author or co-author compliance test plans, protocols, methods, and reports.
  • Support product-safety risk management activities and ensure compliance findings drive appropriate requirements and risk updates.
  • Track compliance status across the program and drive timely resolution of findings.
  • Maintain compliance and product safety documentation within EVR’s quality management system.
  • Communicate with cross-functional stakeholders and provide mentorship on compliance and standards to design engineers.

About the Company

Varian

Tech-enabled radiation oncology hardware and software

Varian, part of Siemens Healthineers, focuses on oncology by providing integrated radiation oncology solutions that combine software, hardware, patient data, and care teams. Its offerings include treatment-planning software, radiation therapy machines, and data-management systems that work together to enable precise cancer treatments. The company differentiates itself through an integrated platform approach and services like Oncology-as-a-Service (OaaS), which lets healthcare providers adopt advanced radiation oncology with ongoing service support rather than large upfront investments. Varian serves healthcare providers such as hospitals and cancer centers, helping them deliver coordinated care and improve patient outcomes. Its goal is to reduce the fear of cancer by using data and technology to support clinicians in delivering effective treatments.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Palo Alto, CA
Founded
1948

Recently Posted Jobs

Explore more opportunities at Varian

See more jobs