Principal Engineer (Systems), MedTech Catapult Productisation Unit
Salary undisclosed
Apply on
Original
Simplified
The MedTech Catapult has a dedicated objective of curating and accelerating the development of high potential MedTech projects through an in-house product engineering unit. This productization unit is responsible for supporting the development of technologies through the medical device development cycle to produce full-fledged hardware product systems. The Principal Engineer will report to Programme Director.
Job Responsibilities
Job Responsibilities
- Lead design teams through full product development from conceptualization to early product production.
- Oversee the technical engineering team and work with cross functional team on the entire implementation relating to hardware, connected devices and related technologies for multiple projects in parallel.
- Guide and lead the development of systems architecture, requirements, specifications and verification reports, in creating hardware product systems that are developed in the productization unit
- Manage feasibility study for each phase on conceptual design for new products and product architecture from conceptualisation to completion
- Ensure product functions meet user expectations, technical requirements and fulfilling budget and quality specifications
- Oversee the analytical studies, verification and validation of the products
- Ensure compliance with the appropriate quality management system and regulatory specifications, and proper document control and communication with internal and external stakeholders
- Providing guidance, mentorship and direction to all engineers and stakeholders on product development
- Guide and oversee the development of system component requirements, interfaces, and specifications necessary to maintain the consistency and integrity of the architectures.
- Provision of technical input to help identify and solve project risks affecting project schedules and plans
- Review and approve documentations for QMS, approve risk analysis, risk management, Verification and Validation procedures.
- Performs hands-on system integration testing and troubleshooting of technical issues.
- Performs system level verification against requirements. Creates test plans, procedures and reports, performs and analyzes system set up, and conducts verification and validation activities.
- Identify and implement product design changes as required for individual products in accordance with internal and external stakeholders.
- Interface with external parties (design houses) to communicate product requirements, and subsequent knowledge transfer to build internal capability
- Masters in System Engineering, Electro-mechanical or related discipline
- >15 years experience in medical devices (e.g. hardware, connected devices) managing product design and development, with hands-on experience in system architecture and integration of mechatronic and software systems
- Experience in Systems Engineering as related to stakeholder needs definition, creation of use case workflows, requirements definition and decomposition, functional architecture, and system design.
- Experience generating technical documentation such as product requirements, specifications, engineering reports, test plans & procedures, validation plans and reports
- Outstanding communication and presentation skills (written and verbal) to all levels of an organization.
- Strong track record of technical leadership and working in cross-functional teams.
- Lead and coordinate with remote development teams
- Ability to work on multiple projects simultaneously
- Enjoy working in a small team, start-up environment
Similar Jobs