NordicNeuroLab AS

Join NordicNeuroLab and help ensure the quality of innovative medical technology used by hospitals and research institutions worldwide.​   Headquartered in Bergen, Norway, NordicNeuroLab is an international and growing company with ambitious plans. We are now looking for a detail-oriented and structured QA Technician to strengthen their team.   About the Role​ As a QA Technician, you will play a key role in ensuring that materials, components, and products meet established quality requirements before they reach NordicNeuroLabs’ customers. You will work closely with Production, Engineering, and Quality functions to maintain high standards of quality, traceability, and compliance. This is a hands-on role for someone who enjoys working with documentation, inspections, quality control activities, and continuous improvement in a production environment.   Key Responsibilities​ • Perform incoming inspections of components, assemblies, and materials. • Conduct visual and mechanical inspections of PCBAs, electronic components, optical parts, and mechanical parts. • Perform functional testing of products and assemblies according to established procedures prior to release. • Review production documentation and Device Production Records (DPRs) to ensure accuracy and traceability. • Identify, document, and follow up quality deviations and non-conformances (NCRs). • Support root cause investigations and corrective actions in production related areas. • Ensure manufacturing and inspection activities are performed according to approved procedures. • Support calibration and maintenance activities for production and test equipment. • Assist with environmental monitoring activities where applicable. • Contribute to continuous improvement of quality processes and documentation. • Work closely with Production and Quality teams to maintain compliance and product quality.   Qualifications​ Required​ • Technical education, vocational training, or relevant practical experience. • Experience working in a manufacturing, production, QA, or QC environment. • Experience performing inspections, quality checks, or documentation review. • Ability to read and follow procedures, specifications, and technical documentation. • Strong attention to detail and a structured way of working. • Good written and verbal communication skills in English. • Ability to work independently while collaborating effectively with cross-functional teams.   Preferred​ • Experience as a QA Technician, QC Technician, Quality Inspector, or similar role. • Experience from regulated industries such as Medical Devices, Electronics, Pharmaceuticals, Aerospace, Automotive, or related sectors. • Experience with ERP, eQMS, or other quality management systems. • Knowledge of NCR handling, traceability requirements, and quality documentation. • Experience inspecting electronic products, PCBAs, or technical assemblies.  • Familiarity with IPC-A-610 standards. • Experience using inspection and measurement tools such as calipers, micrometers, multimeters, oscilloscopes and spectrum analyzer or microscopes.   Who We Are Looking For​ We believe the right person for this role:​ • Has exceptional attention to detail. • Is highly organized and structured. • Enjoys working with documentation and quality processes. • Has the confidence to challenge deviations from procedures when necessary. • Takes pride in accuracy and quality. • Is proactive, dependable, and solution oriented. • Thrives in an environment where quality and compliance are essential.   Why Join NordicNeuroLab?​ • Work with innovative medical technology products used worldwide. • Join an international company with ambitious growth plans. • Be part of a collaborative environment where engineering, quality, and innovation work closely together. • Help shape a newly established role with significant influence and development opportunities. · Work alongside experienced specialists in Quality, Regulatory Affairs, and Engineering. • Contribute directly to patient-focused technology that makes a difference globally.   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   Since its establishment in 2004, Folk AS has assisted both Norwegian and international companies in finding highly skilled professionals within technical and administrative disciplines for project-based, temporary, and permanent positions. This is what we do best, and where our expertise lies. Our core values are: ethical, personal, committed, and flexible.​   We see opportunities in your competence!​

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   Since its establishment in 2004, Folk AS has assisted both Norwegian and international companies in finding highly skilled professionals within technical and administrative disciplines for project-based, temporary, and permanent positions. This is what we do best, and where our expertise lies. Our core values are: ethical, personal, committed, and flexible.​   We see opportunities in your competence!​