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Passionate Medical Device Engineer

Arbeidsgiver

Viking Arm Medical AS

Sted

0357 Oslo

Om jobben

Stillingstittel
Senior Medical Device Engineer
Type ansettelse
Fast, heltid 100%
Arbeidsspråk
Engelsk
Antall stillinger
1

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About Viking Arm Medical

Viking Arm Medical is a Norwegian start-up at the forefront of Thoracic surgery innovation. We develop next-generation surgical retractors and related products to improve surgical ergonomics, enhance procedural efficiency and optimize recovery for patients. Operating under ISO 13485 and EU MDR principles with a network of qualified subcontractors, we have several novel products in the pipeline and a lean Research & Development program.

Position Summary

We seek an experienced, self-driven Medical Device Engineer who can strengthen our engineering team by supporting product development and regulatory readiness and managing vendor compliance, in a dynamic start-up environment. This role will evolve from hands-on product development support to full supply-chain leadership as the company scales toward production and regulatory submission. This position reports to the CTO , and is based at VAM’s office in Oslo. The candidate is willing to travel internationally from time to time.

Key Tasks and Responsibilities

  • Develop and execute device assembly and internal mechanical and functional testing

  • Develop and manage verification and validation activities

  • Draft protocols and reports

  • Create assemblies/fixtures and perform testing of the VAM retractor

  • Handle daily coordination with test houses

  • Maintain DHF and risk documentation updates

  • Support design iteration and troubleshooting and technical problem-solving

  • Take over BOM maintenance and lab-related operational tasks

Qualifications & Experience

  • Bachelor’s degree in engineering, an advanced degree and CAD fluency (e.g. SolidWorks) are plusses.

  • At least 5 years’ experience in regulated Medical Device Product Development and manufacturing with deep knowledge of ISO 13485, and EU MDR and/or FDA 21 CFR Part 820 requirements.

  • Proven success in supplier development, process qualification (IQ/OQ/PQ) and contract manufacturing operations.

  • Strong understanding of risk management, quality control and statistical/lean methods (e.g., Six Sigma, DMAIC).

  • Communicate effectively with vendors and internal stakeholders and manage complex supply-chain projects.

  • Fluent (Verbal, R&R) English

Personal Attributes

  • Structured, detail-oriented and accountable, with a strong sense of ownership of product Development and supply-chain and production/ processes.

  • Hands-on problem solver who thrives in a fast-moving start-up environment and can adapt to changing priorities.

  • Excellent communicator who can build partnerships with suppliers and internal stakeholders.

  • Committed to maintaining high standards of quality, traceability and regulatory compliance.

What we offer

  • The opportunity to work in, and be part of a fast-growing start-up company, developing and launching Disruptive, Patented Medical Devices.

  • Personal growth and career development potential in a Global environment

  • A competitive package including a performance-based stock option plan.

How to Apply

To join our mission of transforming thoracic surgery, please send your CV and a cover letter detailing your relevant experience and why you are a great fit for Viking Arm Medical’s Engineering team role. We look forward to hearing from you and working together to bring our innovative products to market.

Please send your job-application and CV in english to our CTO: Hans Martin Aguilera

Om bedriften

Sektor

Privat

Del annonsen

Annonsedata

Rapporter annonse
Stillingsnummer

e6f364c0-cf08-4050-ae98-8b9b4169bcf9

Sist endret

18. februar 2026

Hentet fra

FINN

Referanse

450852993

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