Overview
As a Senior Electronics Engineer, you will lead electronic design activities for medical devices that meet ISO 13485 standards and help take products to market. You will work within a cross-functional team of engineers and scientists to drive development, quality, and regulatory alignment. The role includes some project management responsibilities and regular updates to internal and external stakeholders. This is a growth-focused opportunity at a company delivering innovative healthcare technology with strong regulatory involvement.
Pay / Benefits
- starting salary
- pension
- bonus
- shares purchase scheme
- private healthcare
- career development
Responsibilities
- Lead electronics design for medical devices to ISO 13485 standards
- Collaborate with software, embedded, mechanical, and regulatory teams
- Contribute to product development from concept to market release
- Communicate progress and risks to internal and external stakeholders (project management)
- Support regulatory compliance activities and design reviews
- Participate in cross-functional planning and technical decision-making
- Mentor junior engineers and promote best practices in electronics design
Key requirements
- Proven track record developing medical devices that reached market with electronics design under ISO 13485
- Experience in cross-functional collaboration across hardware, software, and regulatory teams
- Ability to relay information to internal and external teams (project management experience)
- Desirable knowledge of EN 60601 standards
- Degree from a leading university (field unspecified) with relevant industry experience
- Availability to start soon
- strong communication
- cross-functional collaboration
- problem-solving
- electronics design for medical devices
- ISO 13485 compliance
- regulatory understanding for medical devices
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