Company Description
We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
Are you ready to take your career to the next level? If you have a strong background as a Product Assessor within an EU notified body conducting MDD/MDR technical documentation review, then we have an exhilarating opportunity for you! Join our dynamic team at SGS and become a Senior Product Assessor - Active Devices. This role will allow you to make a significant impact in the field of certification.
As a member of our Medical Device team, you will manage a small team of globally based Product Assessors and dive deep into the exciting world of Active Medical Devices.
Your responsibilities will include: Supporting and guiding your team of talented Product Assessors.Conducting thorough technical documentation reviews and ensuring compliance with EU regulations and standards.Collaborating with cross-functional teams to increase efficiency and quality.Monitoring the team's technical competence, KPIs, and wellbeing and providing feedback and support when there are concerns.Conducting recruitment, including reviewing CVs and undertaking interviews, and supporting with onboarding of new starters.Developing training and presenting the training to others in SGS or externally as deemed necessary.Assisting with technical queries and those related to sales within the Active Medical Devices field.Ensuring that the highest level of service is provided throughout the SGS network offering medical devices certification and stakeholders through efficient service delivery.Qualifications
To be eligible for this role, you should have prior experience as a Product Assessor/Specialist/Technical File Reviewer within another Notified Body for active devices, conducting reviews against MDD and/or MDR.
Additionally, you must possess:
Four years of professional experience in the field of healthcare products or related activities, such as design, manufacturing, auditing, or research, of which two years shall be in the design, manufacture, testing, or use of the device or technology to be assessed or related to the scientific aspects to be assessed.Active Medical Devices knowledge (monitoring equipment, therapeutic devices, devices utilizing radiation, stand-alone software devices, etc.) through designing, manufacturing, or testing of such devices.Thorough knowledge and understanding of related standards: EN 60601, EN 62304, EN 62366, etc.Good written English skills (as reports will be reviewed/queried in English); Knowledge of the following Technical File codes desirable (as per COMMISSION IMPLEMENTING REGULATION (EU) 2017/2185 of 23 November 2017): MDA0201, MDA0202, MDA0203, MDA0204, MDA0301, MDA0302, MDA0303, MDA0304, MDA0305, MDA0306, MDA0307, MDA0308, MDA0309, MDA0310, MDA0311, MDA0312, MDA0313, MDA0314, MDA0315, MDA0316, MDA0317, and MDA0318.Additional Information
Why SGS?
Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry.Enjoy a flexible schedule and remote 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.Join Us: 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. Apply now to be part of our motivated and dynamic team!
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