At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
Roche Diabetes Care is committed to helping people with diabetes live their lives.
As a pioneer in the development of blood glucose monitoring and insulin delivery systems, we want our patients to be as active as possible and help healthcare professionals manage their patients' condition in an optimal way. The ACCU-CHEK® portfolio-from blood glucose monitoring through information management to insulin delivery - offers innovative products, services and comprehensive solutions for convenient, efficient and effective diabetes management.
As a Senior Test Engineer, you will bridge the gap between scientific/clinical requirements and robust, life-changing hardware solutions. You will lead verification activities, tackle complex system-level challenges, and provide technical mentorship in a dynamic, cross-functional environment.
You will provide high-level testing expertise to support product and lifecycle management. You will define and implement test strategies at the program level and across multiple scrum teams.
You will lead submission and certification strategies for our CGM & BGM systems to ensure global market access.
You will serve as the subject matter expert for Electromagnetic Compatibility (EMC) and Electromagnetic Voltage (EMV) testing, ensuring wearable devices meet all regulatory standards.
You will define, mandate, and oversee complex work packages for external partners, including accredited laboratories, certification bodies, and national authorities.
You will execute rigorous testing and evaluate results to assess product maturity. Ensure all verification content is "state-of-the-art" and compliant with international medical standards.
You will act as a bridge between the user and the lab; translate customer usage data and market feedback into design improvements to enhance product reliability.
You will modernize verification methods and automated test setups, supporting their continuous evolution to maintain a competitive technological edge.
You will support product care and quality functions by leading detailed technical investigations into market complaints and field performance.
This is an on-site position based in Indianapolis, IN.
Relocation benefits are not being offered for this role.
Who You Are:
(Required)
You have a Bachelor’s in Mechanical Engineering, Mechatronics, Electronics, or a related technical discipline with 7+ years of relevant experience, or Master of Science in Mechanical Engineering, Mechatronics, Electronics, or a related technical discipline with 5+ years of relevant experience
You have demonstrated experience in medical device verification, ideally within In-Vitro Diagnostics (IVD) or complex diagnostic instruments.
You have a high level of technical proficiency / "hands-on" expertise in hardware testing (e.g., PCBAs, sensors, battery life) and a strong conceptual understanding of embedded systems.
You have a solid understanding of regulatory knowledge, understanding the international standards for medical electrical equipment and the documentation required for regulatory submissions.
Preferred:
You have an advanced degree with 5+ years in the pharmaceutical/diagnostic space
You have demonstrated experience working in and outside of the lab; working closely with engineers and other stakeholders
You are a proactive problem-solver who thrives on complexity, possesses a keen eye for detail, and can work independently within a collaborative framework.
You have experience supporting the development of a commercialized instrument/device.
You have demonstrated strong interpersonal and communication skills with the ability to communicate technical knowledge in a clear and understandable manner, especially to non-experts; you excel at problem-solving skills and the ability to work under ambiguous situations.
You have excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple changing projects and priorities; you complete work in a timely, accurate and thorough manner.
The expected salary range for this position based on the primary location of Indianapolis, IN is $112,000 - $208,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
This position also qualifies for the benefits detailed at the link provided below.
Benefits
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.