Senior Product Assessor - Active Devices
Full-time
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.
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.
Your responsibilities will include:
Supporting and guiding your team of talented Product AssessorsConducting thorough technical documentation reviews and ensuring compliance with EU regulations and standards.Collaborating with cross-functional teams to increase efficiency and qualityMonitoring the team's technical competence, KPIs, and wellbeing and providing feedback and support when there are concerns.Conduct recruitment, including reviewing CVs and undertaking interviews and supporting with onboarding of new startersDevelop training and present the training to others in SGS or externally as deemed necessary.Assist with technical queries and those related to sales within the Active Medical Devices field.Ensure that the highest level of service is provided throughout the SGS network offering medical devices certification and stakeholders through efficient service delivery.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.
#J-18808-Ljbffr