Product Compliance Specialist

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

The Product Compliance Specialist is responsible for ensuring global product compliance and certification throughout the product lifecycle, from concept and development through commercialization and obsolescence. This role serves as the subject matter expert for product safety, EMC, and applicable regulatory standards, partnering closely with Engineering, Quality, Regulatory Affairs, and external certification agencies to maintain compliance for medical device products.

The Product Compliance Specialist provides technical guidance on safety and EMC requirements, supports risk management activities, coordinates regulatory and certification testing, and ensures products meet applicable global standards and regulatory requirements.

Product Safety & EMC Compliance

• Determine applicable regulatory requirements and standards for new and existing products.
• Provide product safety and EMC guidance based on standards expertise, interpretation, and research.
• Support safety and EMC investigations throughout the product lifecycle.
• Communicate compliance requirements and design considerations to cross-functional and hardware engineering teams.
• Participate in risk management reviews and product safety assessments.
• Support compliance activities from product development through end-of-life.
  

Regulatory & Certification Management

• Coordinate testing activities with third-party laboratories and certification bodies.
• Support global product approvals and ongoing certification maintenance.
• Assist with regulatory agency inspections and quarterly Follow-Up Services (FUS) activities.
• Maintain compliance records, certifications, and technical documentation.
• Ensure continued compliance with applicable global regulatory and industry standards.
  

Cross-Functional Partnership

• Work closely with Engineering, Quality, Regulatory Affairs, and Product Management teams.
• Communicate compliance status, test results, and certification updates throughout all design phases.
• Provide technical recommendations related to product safety, EMC, and certification requirements.
• Support issue resolution related to product compliance and certification activities.
  

Standards & Technical Expertise

• Apply expertise in medical electrical safety and EMC standards to support product development efforts.
• Interpret standards requirements and translate them into actionable technical requirements.
• Support compliance strategies for new product introductions and design changes.
• Assist with investigations related to EMC, EMI, and product safety concerns.
  

Required Qualifications

• Bachelor's degree in Electrical Engineering, Mechanical Engineering, or a related technical discipline.
• 5+ years of experience in product compliance, EMC, electrical safety, or related compliance functions.
• Experience managing product compliance activities and obtaining global certifications.
• Experience working with medical electrical safety and EMC standards, including: IEC 60601-1 IEC 60601-1-2 IEC 60601-2-1
• Proven experience obtaining NRTL approvals for medical devices.
• Knowledge of electronics, mechanical design, and product safety principles.
• Experience working with third-party testing and certification laboratories.
• Experience developing and documenting technical requirements based on regulatory and industry standards.
• Proficiency with Microsoft Office applications, including Excel.
  

Preferred Qualifications

• Master's degree in Electrical Engineering, Mechanical Engineering, or related technical field.
• Experience troubleshooting EMC/EMI hardware issues.
• Experience with FDA guidance and regulatory requirements for medical devices.
• Knowledge of laser safety requirements and compliance standards.
• Experience conducting medical device safety risk assessments.
• Strong analytical and problem-solving skills, including statistical analysis.
• Excellent communication and cross-functional collaboration skills.

Additional Information

• Based in Palo Alto, California.
• Hybrid work environment with onsite collaboration required several days per week.
• Approximately 10% international travel as needed.
• Opportunity to support innovative medical technologies as part of Varian, a Siemens Healthineers company.

#LS-OS1

Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

To find out more about Siemens Healthineers businesses, please visit our company page here.

The base pay range for this position is:

Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here.

Export Control: “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”

Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.

Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.

To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.