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Senior Consultant at STR Group AG | Partnering with Businesses in Switzerland for Talent Acquisition & Growth
A leading manufacturer in the field of advanced medical solutions, specializing in sophisticated critical care and emergency transport systems, is seeking a highly skilled System Engineer. Our innovative solutions cater to a diverse range of patient demographics and clinical environments, including intensive care, critical transport, and specialized imaging facilities.
We are seeking a System Engineer who excels in a collaborative environment and is committed to upholding rigorous standards. This role presents a unique opportunity to contribute to the development of next-generation medical technology. You will be instrumental in guiding complex systems from their initial conceptualization through to market readiness, with an unwavering focus on quality, patient safety, and regulatory compliance.
Responsibilities
* Define robust and secure system architectures that address clinical requirements, stakeholder expectations, and regulatory mandates, while maintaining a practical perspective on feasibility and value.
* You will lead the complete system lifecycle, encompassing requirements definition, integration, and validation, ensuring adherence to safety protocols, usability standards, and project timelines.
* Work closely with project managers, engineering disciplines, and regulatory affairs specialists to translate conceptual designs into fully realized, standards-compliant products.
* Facilitate integration and verification planning with a pragmatic approach to relevant medical device regulations, including but not limited to, MDR, FDA, ISO 13485, and IEC 60601.
* Enhance traceability and efficiency within engineering processes through the strategic implementation of modern Application Lifecycle Management (ALM) tools and adherence to best practices in requirements and test engineering.
Profile
* An academic qualification in engineering or a closely related technical discipline (e.g., B.Sc. FH, M.Sc. ETH, or equivalent).
* Demonstrable experience, acquired over several years, in the development of medical devices or within other highly regulated industries.
* Proven ability to integrate deep technical expertise with effective decision-making to maintain project momentum.
* A proactive mindset with a strong commitment to continuous improvement, evidenced by a willingness to propose, shape, and implement process enhancements.
* Exceptional communication skills and a pragmatic approach to problem-solving, thriving in interdisciplinary team settings.
* Familiarity with regulatory standards is advantageous; a willingness to develop expertise in this area is essential. Prior experience with MDR, ISO 13485, FDA, or IEC 60601 is considered a plus.
* Proof of eligibility to work in Switzerland is required, sponsorship is not offered.
* Proficiency in English is required; fluency in German is a significant advantage.
Corporate Culture and Benefits
We foster a cooperative and grounded work environment, characterized by mutual respect and open communication. Our commitment extends beyond a stimulating professional setting to encompass various leisure activities and contemporary working conditions. We believe in interactions at eye level, promoting a pleasant and productive atmosphere. Join a team where your expertise is highly valued and innovative contributions are actively encouraged.
Should you wish to apply, please submit your application online or email me directly ben@strgroup.ch
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Information Technology, Engineering, and Research
* Industries
Medical Equipment Manufacturing
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