Product Assessor Orthopaedic; Notified Body

As a Product Assessor, you will play a pivotal role in conducting orthopaedic product assessments and technical documentation reviews in strict adherence to European Medical Device Regulation (EU MDR 2017/745) and the UK Medical Device Regulation (UK MDR 2002) and for Class IIa/IIb and/or Class III devices.

• Conduct thorough technical and clinical assessments of non-active orthopaedic medical devices under relevant commission regulation codes, with potential to extend expertise to dental devices.
• Identify and rectify instances where device technical documentation deviates from compliance with applicable requirements.
• Provide support for CE and UKCA marking activities within SGS.
• Contribute to the training and qualification of junior staff and develop comprehensive training materials.
• Communicate effectively with team members, clients, and other stakeholders regarding product assessments, working diligently to minimise regulatory risks associated with medical device certification.
• Ensuring diligent management of scheduled work to maintain timeliness and efficiency in deliverables.

• 4+ years of professional experience in the orthopaedic products sector or related fields, covering roles in design, manufacturing, auditing, or research. Crucially, a minimum of two years should be directly involved in the design, manufacturing, and testing of orthopaedic products, or in roles that require a deep understanding of the scientific principles underlying these products or technologies.
• Understanding of essential standards for orthopaedic products.
• Prior experience in conducting orthopaedic product assessments for a Certification/Notified Body (acting as a Technical Documentation Reviewer) is advantageous.
• A Master's degree, PhD, or equivalent in a related discipline, such as medicine, biomedical engineering, or biomedical science, preferably with a focus on orthopaedic devices.
• Proficiency in modern electronic communication platforms.
• Strong written English skills essential for reviewing and querying Technical Documentation assessment reports.
• Demonstrated ability to learn independently.
• Desirable:
  Regulatory Acumen - knowledge of the European Medical Device Regulation (EU MDR 2017/745) and the UK Medical Device Regulation (UK MDR 2002) and familiarity with medical device codes MDA/MDN/MDS for MDR as outlined in Commission Implementing Regulation (EU) 2017/2185.

Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry.

Enjoy a flexible schedule and work model.

Access SGS University and Campus for continuous learning options.

Thrive in a multinational environment, collaborating with colleagues from multiple continents.

Benefit from our comprehensive benefits platform.

At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. We value diversity and provide endless opportunities to learn, grow your expertise, and fulfill your potential.

The role is fully remote.