Senior Regulatory Affairs Engineer (TCI) at Neko Health - Europe | $120,000 - $150,000

Are you ready to shape the future of medical technology? Neko Health is seeking a Senior Regulatory Affairs Engineerwho’s passionate about tackling complex regulatory strategies, enjoys working with cutting-edge medical devices, and thrives in a fast-paced, collaborativeand distributed environment.

We are looking for you that have extensive experience from working with active medical devices and software as a medical device throughout the product lifecycle.

What You’ll Do

Drive Regulatory Excellence: Ensure our cutting-edge medical devices meet global standards and regulations as well as align with regulatory strategies from research and development to market launch and post-market.

Support Product Development: Advise on regulatory strategy throughout the product lifecycle, influencing design, risk management, supplier selection, and device labeling.

Maintain Regulatory Documentation: Develop and maintain regulatory documentation, including Design History File (DHF), Technical Documentation, as well as Device Master Record (DMR) and Device History Records (DHR).

Own Regulatory Submissions: Prepare, review, and submit documentation for EU MDR, FDA, and other international markets.

Monitor Product Safety: Participate in post-market surveillance, CAPA, and complaint management activities.

Interact withRegulatory Bodies: Coordinate communications with regulatory bodies and drive certification projects and vigilance activities, ensuring timely reporting and compliance.

Empower Process Owners and Teams: Guide process owners and product teams to integrate regulatory requirements into our Quality Management System and deliver impactful training on compliance and regulatory topics.

Stay Ahead: Monitor regulatory trends and provide intelligence to keep Neko Health at the forefront of compliance.

What You Bring

Education: BSc or MSc in law, medicine, pharmacy, engineering, or a related field.

Experience: 4–5+ years in regulatory affairs or quality management for active medical devices and software as a medical device.

Expertise: Deep knowledge of EU MDR, FDA CFR (Title 21 Subchapter H), UK MDR, ISO 13485, IEC 60601-1, IEC 62304, ISO 14971, and more.

Skills: Analytical, detail-oriented, and able to interpret complex regulations to provide risk-based recommendations.

Communication: Excellent interpersonal and writing skills; able to engage and inspire both internal teams and external stakeholders.

Mindset: Self-motivated, independent, and ready to take ownership in a dynamic, quality-focused environment.

Languages: Fluent English required; Swedish proficiency is a plus.

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