Assessor & Technical Reviewer, Non-Active and Active Medical Devices
DNV
Job Description:DNV Product Assurance AS is a designated Notified Body for Medical Device Regulation and in process to be designated Notified Body for In-Vitro Diagnostic Regulation, Accredited Certification Body for ISO 13485 and Recognized Auditing Organization under MDSAP. We provide global market access by certifying the safety and quality of products and systems to international safety and quality standards and regulations. Our high professional standards and our sustainable approach guarantee you a forward-thinking work environment, within an organization that invests in its employees, and is committed to providing you with continued development.Are you an experienced professional in medical devices looking to make a real impact? At DNV, we are seeking a highly skilled Medical Device Assessor and Technical Reviewer to join our team of experts. In this role, you will be at the forefront of ensuring medical devices meet the highest regulatory and safety standards.As part of our team, you will conduct in-depth assessments of technical documentation for both active and non-active medical devices, ensuring full compliance with MDR and internal quality standards. You will also play a key role in reviewing assessment reports and collaborating with internal assessors and customers to address technical challenges.What You’ll Be Doing:
Responsibilities:
DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity.Qualifications:What We’re Looking For:
Biology, Microbiology, Biomechanical Engineering, Dentistry, Material/Biomaterial Science, Chemistry, Physics/Biophysics, Medical Technology, Pharmacy, Electrical, Electronics, Mechanical, or Bioengineering, Software Technology/AI, and more.Experience:
Skills:
If you are ready to take your expertise to the next level and contribute to the safety of medical devices worldwide, we want to hear from you.Apply today and help shape the future of medical device compliance.Application deadline: 15th of April, 2025.
Norge
Wed, 26 Mar 2025 02:07:11 GMT
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