Senior Testing Engineer

About the company SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.  Job Overview As a Senior Test Engineer, you will play a critical role in ensuring the robustness and compliance of medical device designs through rigorous assessments and innovative testing methods. You will collaborate with cross-functional teams, serve as a subject matter expert in test case design, and apply statistical problem-solving techniques to drive continuous improvement. This position offers the opportunity to contribute to the development of high-quality medical devices that meet stringent industry standards. Main Responsibilities Ensure robust medical device designs through early and rigorous design assessments. Ensure compliance with engineering principles, company standards, customer requirements, and related specifications. Develop test methods for design assessment, verification and high-volume production, including test design and mechanical/dynamical fixture development. Write and execute design assessment and engineering test protocols; analyze data and author test reports for the design history file. Interact with internal stakeholders from various departments to test products and develop fixtures. Collaborate with the development team to clarify design inputs and enhance testability. Apply statistical methods and problem-solving techniques (e.g., fishbone diagrams, 5 Whys, DMAIC) in investigations and experimental work. Support the development of innovative methods and models to assess device robustness. Take on additional responsibilities as needed to contribute to team objectives Minimum Requirements 5+ years of experience writing verification test plans and protocols, and completing test reports Previous experience in the medical device or pharma industry, ideally with working knowledge of regulations and standards such as 21 CFR Part 820, ISO 13485, ISO 11608, ISO 14971 Master's degree in Mechanical-, Material-, and, Biomedical Engineering or similar Fluency in English Preferred Requirements Previous experience working with injection molded plastics Previous experience in the design and development of medical diagnostic or drug delivery equipment is preferred Good understanding of testing and analytical methodologies Previous…