Senior Development Engineer / MedTech

Senior Development Engineer for MEQU A/S - Compliance & Verification

Join a fast-growing MedTech company in Copenhagen

Become part of MEQU's R &D team and play a key role in bringing new innovative medical devices from development to market.

°MEQU is expanding, and we are looking for a Senior Development Engineer to join our R&D team and support the continued development of our °M Warmer System – a portable blood and IV fluid warmer used in critical care settings worldwide.

About °MEQU

At °MEQU, we empower healthcare professionals to fight hypothermia and save lives. Our °M Warmer System heats fluids to body temperature within seconds and is trusted by military forces, emergency services, and hospitals globally. With CE-marking since 2018 and FDA 510(k) clearance in 2024, we’re now scaling up and entering new markets.

Our Danish office is located at Symbion, Fruebjergvej 3, 2100 Østerbro, Copenhagen.

About the position

This is a newly created position designed to complement our existing product development capacity. You will bridge standards, product requirements, verification activities and technical documentation while supporting a wide range of R &D activities across the product lifecycle.

Key Areas of Responsibility for the position as Senior Development Engineer

• Standards interpretation and compliance activities
• Requirement analysis and traceability
• Verification planning, execution and reporting
• Technical documentation and Design Control deliverables
• Labeling and IFU development
• Support the product integration between R &D functional areas
• Risk Management support
• Design Reviews and Change Control
• Cross-functional collaboration with R &D functions but also operations and QA/RA.

About You

It is important that you meet these Qualifications:

• A degree in a relevant Engineering Field (BSc, MSc, or equivalent)
• Experience with Medical Device development
• Experience with verification and validation activities
• Experience working in an ISO 13485 environment

Besides this, it will be an advantage if you have worked with the following:

· Risk management (ISO 14971)

· Electric Safety (IEC 60601)

· Usability engineering

· Statistics and data analysis

· Labelling and regulatory documentation

· Technical writing and documentation

As a person you are characterized by

• Being a Hands-on problem solver with a structured approach to your work
• Having strong collaboration and communication skills
• Thriving in a very flexible working environment where change and professional adaptability is called for

What We Offer

• An exciting new position in a team of very professional and competent technical experts
• The possibility to join the fast development of a MedTech company that offers live-saving products to many countries and customers in the world
• A culture of continuous learning, improvement, collaboration and patient-first focus.

As °MEQU continues to grow, your role may evolve – and we see that as an opportunity.

Apply Now

For this recruitment, MEQU work together with an external HR Advisor.

Send your CV and application to [email protected] or use Easy Apply.

For questions about the recruitment process, contact Nils Munck at +45 5357 3274.

For questions about the position, contact Jesper Krogh Christensen, R&D Manager at +45 5117 6778.

We review applications on an ongoing basis, so don’t wait too long to apply.

Deadline for application is September 1st.