Join NordicNeuroLab as an Electrical Compliance Engineer

NordicNeuroLab AS

New Jersey

On-site

USD 73,000 - 104,000

Full time

14 days+
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Job summary

NordicNeuroLab AS in Bergen, Norway seeks an Electrical Compliance Engineer to join the Quality & Regulatory Affairs team, bridging engineering, product development, testing, verification and regulatory compliance.

The role focuses on ensuring products meet international standards, supporting design and certification, and developing audit-ready documentation. The ideal candidate has a strong technical background and interest in standards and product safety.

Qualifications

  • Bachelor's or Master's degree in Electrical Engineering or related discipline.
  • Experience with standards, compliance, certification and testing.
  • Strong technical writing and audit-ready documentation.

Responsibilities

  • Interpret and apply international standards for electrical products.
  • Translate regulatory requirements into design, testing, verification, validation activities.
  • Review designs, test plans, and documentation from a compliance perspective.
  • Develop and maintain compliance documentation.

Skills

Electrical engineering
Regulatory compliance
Technical writing
English communication

Education

Bachelor's or Master's degree in Electrical Engineering

Job description

Join NordicNeuroLab as an Electrical Compliance Engineer

5009 Bergen

Stillingstittel Electrical Compliance Engineer

Type ansettelse Fast, heltid 100%

Antall stillinger 1

Frist: Applications are reviewed continuously

Join NordicNeuroLab and help shape the future of medical technology

Headquartered in Bergen, Norway, NordicNeuroLab is an international and growing company with ambitious plans. To support continued growth and increasing regulatory demands, we are now looking for an Electrical Compliance Engineer to join their Quality & Regulatory Affairs team.

About the Role

This is a newly established position that will work closely with the VP Quality & Regulatory Affairs and engineering teams across the organization.

This role bridges engineering, product development, testing, verification and validation, and regulatory compliance. You will help ensure that NNL’s products meet applicable international standards and certification requirements while providing compliance support to engineering teams throughout the product lifecycle.

We are looking for someone who combines strong technical understanding with an interest in standards, compliance, certification, technical documentation, and product safety.

This role offers a unique opportunity to help shape and develop NNLs' compliance capabilities while working with innovative medical technology products used worldwide.

Key Responsibilities
  • Interpret and apply international standards and regulatory requirements for electrical and electronic products.
  • Support engineering teams in translating regulatory requirements into practical design, testing, verification, and validation activities.
  • Review product designs, technical solutions, test plans, and engineering documentation from a compliance perspective.
  • Develop and maintain compliance and traceability documentation.
  • Support verification and validation activities throughout product development and sustaining engineering.
  • Coordinate compliance and certification activities with external laboratories, testing facilities, and certification bodies.
  • Contribute to product risk management activities related to electrical safety and compliance.
  • Support regulatory submissions and technical documentation for global markets.
  • Assess the compliance impact of product changes, component obsolescence, and design updates.
Preferred Background
  • Bachelor's or Master's degree in Electrical Engineering, Electronics Engineering, Automation, Physics, Medical Technology, or related technical discipline.
  • Experience working with standards, compliance, certification, verification, validation, testing, quality, or regulatory activities.
  • Experience with product certification, technical documentation, and engineering documentation.
  • Strong technical writing and documentation skills.
  • Strong written and verbal English communication skills.
Valuable Experience

Experience from the medical device industry is highly desirable, particularly within active medical devices and electrical safety standards.

Knowledge of one or more of the following areas is considered advantageous:

  • Medical electrical equipment standards for safety and Electromagnetic Compatibility (EMC) (IEC 60601 series)
  • Verification and Validation (V&V)
  • ISO 14971 Risk Management and ISO 13485 Quality management system
  • FDA, MDR, or other regulatory frameworks
  • CE marking and product certification processes
  • Wireless product compliance (RED, FCC, ETSI)
  • Environmental compliance requirements (RoHS, REACH, PPWR, WEEE)
  • Product certification processes involving UL, TÜV, CSA, or similar organizations
Who We Are Looking For

The ideal candidate is:

  • Structured, organized, and detail-oriented.
  • Comfortable working with standards, regulations, and technical requirements.
  • A strong technical writer capable of producing clear, accurate, and audit-ready documentation.
  • Able to understand complex technical systems and communicate effectively across disciplines.
  • Self-driven and capable of working independently.
  • Comfortable balancing engineering challenges with regulatory requirements.
  • Motivated by quality, compliance, and continuous improvement.
Why Join NordicNeuroLab?
  • Work with innovative medical technology products used worldwide.
  • Join an international company with ambitious growth plans.
  • Thrive in a collaborative environment where experienced Quality, Regulatory Affairs, and Engineering teams work together to advance innovation.
  • Help shape a newly established role with significant influence and development opportunities.
  • Contribute directly to patient-focused technology that makes a difference globally.

Candidates residing outside Norway are welcome to apply, provided they are willing to relocate to Bergen.

For questions regarding this position, please contact Michelle Kolskår, Head of Sales at Folk AS.
Phone: +47 48 13 66 56
E-mail: michelle@folkas.com

NordicNeuroLab AS (NNL) develops and manufactures advanced solutions for functional MRI (fMRI) studies and patient comfort systems used in MRI environments worldwide. Their products are trusted by hospitals, universities, and research institutions across the globe and play an important role in supporting the diagnosis and treatment of neurological disorders.

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