Test Engineering Manager
Listed on 2026-07-21
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Engineering
Quality Engineering, Regulatory Compliance Specialist
Varian Medical Systems, a Siemens Healthineers company, is seeking a Test Engineering Manager to join our Interventional Oncology (IO) development team. The role involves leading the testing aspects of design and development related to new implantable therapy and embolization products, and managing a team of laboratory technicians.
What You will do- Develop and execute complex test plans involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
- Lead coordination with external testing agencies and laboratories to evaluate devices
- Support design and development of novel chemical and materials-based devices, including chemical (XRD, DSC, leachable, etc), radiation-related, and mechanical (stiffness, sizing, etc) assessments
- Develop validated methods for process development and production needs for both internal and external testing
- Write technical documentation including process descriptions and test methods
- Lead the R&D team of laboratory technicians including hiring, performance management, and training
- Manage technician resources within and across projects to reach program goals
- Provide technical leadership and guidance to the project team
- Mentortechniciansin best practices
- Contribute to and maintain FDA compliant Design History Files (DHF)
- Execute test processes as they relate to quality system compliance with FDA 510(K), QSR and ISO 13485
- Participate in complaint investigations, and failure analysis of products
- Provide root cause analysis support and drive the implementation of corrective action for process-related issues
- Perform other duties as assigned or required
- Bachelor's degree in Chemical Engineering, Biomedical Engineering, Materials Science, or a related technical field
- 5+ years of experience in test engineering, materials characterization, or laboratory-based product testing
- 2+ years of experience leading, mentoring, or supervising laboratory or engineering staff
- Hands-on experience with chemical, materials, and/or mechanical testing and test method development or validation
- Experience managing or coordinating work with external testing laboratories or vendors
- Working knowledge of regulated product development environments (e.g., FDA, ISO 13485, QSR, or similar)
- Experience supporting design verification and validation activities
- Ability to work effectively within a documented Quality System
- Strong organizational skills with attention to detail and data quality
- Effective communication skills, both written and verbal
- Master's degree or PhD in a relevant engineering or scientific discipline
- Experience developing or testing regulated medical devices and/or combination products
- Exposure to radiation-based testing or evaluation methods
- Prior laboratory or engineering management experience within a medical device or similarly regulated industry
The base pay range for this position is: $104,930 - $144,276.
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 disability insurance
- short‑term disability insurance
- paid parking/public transportation
- paid time off
- paid sick and safe time
Siemens Healthineers is an Equal Opportunity and Aff… 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.
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Reasonable AccommodationsSiemens 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.
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