Engineer II, Systems - Defined Term

Position: Engineer II, Systems  - Defined Term
With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career?

You just found it.

Job Overview The Systems Engineer will be responsible for providing technical input to a team of systems and cross-functional engineers. You will support the development, improvement, verification, and troubleshooting of on-market electromechanical medical devices, including hands-on work in the engineering lab to support testing, data collection, and root cause assessment. A key aspect of this role involves the use of tools such as Excel and JAMA for requirements management and traceability, ensuring that all project deliverables meet the specified criteria.

The ideal candidate will support implementation of changes and is capable of working with a degree of flexibility while maintaining the current product and driving improvements in our systems engineering practices. The systems engineer will ensure that development, remediation, and investigation activities are compliant with internal development processes and regulatory requirements specifically 21 CFR 820.30.

Job Responsibilities and Essential Duties Support the development and improvement of on-market electromechanical medical devices, ensuring that solutions are scalable, maintainable, and meet regulatory requirements.

Utilize tools such as Excel and JAMA to manage requirements, track progress, and ensure traceability throughout the project.

Work in the engineering lab to support system-level testing, troubleshooting, data collection, test setup execution, and root cause assessment for product issues, complaints, CAPAs, and design changes.

Collaborate with cross-functional teams to define project scope, objectives, and deliverables.

Participate in design reviews and provide constructive feedback to team members to ensure high-quality designs.

Maintain the current product while implementing innovative solutions and improvements.

Support the development and remediation of electromechanical medical devices, ensuring that solutions are scalable, maintainable, and meet regulatory requirements.

Collaborate with cross-functional teams to define project scope, objectives, and deliverables.

Participate in design reviews and provide constructive feedback to team members to ensure high-quality designs.

Maintain the current product while implementing innovative solutions and improvements.

Drive product improvements based on data and feedback.

Ensure compliance with all relevant regulatory requirements and standards.

Minimum Requirements BS in Systems, Biomedical, Electrical, Software, or related Engineering discipline with 3+ years of related systems engineering, design controls, medical device, product development, engineering lab testing, or root cause investigation experience MS or PhD in Systems, Biomedical, Electrical, Software, or related Engineering discipline with 2+ years of related systems engineering, design controls, medical device, product development, engineering lab testing, or root cause investigation experience

Required Knowledge, Skills, and Abilities Demonstrated ability to work with moderate independence in regulated product development, system-level testing, troubleshooting, objective evidence collection, and root cause assessment.

Strong track record of supporting the development of electromechanical medical devices.

Proficiency in using tools such as JAMA for requirements management and traceability.

Strong understanding of…