Senior Hardware Engineer, Medical Devices

Dignio; Oslo; On-site; NOK 900,000 - 1,300,000; Full time

Job summary

Dignio is seeking a Senior Hardware Engineer to drive the electronics in connected medication dispensers. You will take designs from architecture through schematic, layout, and prototyping into volume production with manufacturing partners, and collaborate with test, software, and mechanical teams.

You will ensure regulatory compliance, maintain documentation, and manage design changes while focusing on patient safety and product quality.

Qualifications

• Substantial experience designing electronics that have shipped in volume.
• Experience taking designs into production through contract manufacturers.
• Good understanding of wireless connectivity and EMC design considerations.
• Experience with regulatory and certification processes for medical devices or safety-critical fields.

Responsibilities

• Design schematics and PCB layouts for reliable, manufacturable circuit boards.
• Select and qualify components focusing on long-term availability, cost and performance.
• Build and test prototypes to validate functionality and reliability.
• Contribute to certification and regulatory testing, addressing EMI/EMC and safety.
• Prepare manufacturing documentation and coordinate with contract manufacturers.
• Manage design changes with impact on safety, performance and risk.
• Collaborate with embedded software, mechanical, and test engineers to integrate hardware into final products.
• Maintain hardware design records in a PLM system for traceability and compliance.

Skills

Electronics design

PCB layout

Schematic capture

Hardware validation

Contract manufacturing support

Wireless connectivity

EMC design

Tools

PLM system

Job description

Dignio is seeking a Senior Hardware Engineer to drive the electronics in connected medication dispensers. You will take designs from architecture through schematic, layout, and prototyping into volume production with manufacturing partners, and collaborate with test, software, and mechanical teams.

You will ensure regulatory compliance, maintain documentation, and manage design changes while focusing on patient safety and product quality.