Auditor Medical Devices

2 maanden geleden

Rotterdam, Nederland LRQA Voltijd

Job ID:
Location:Rotterdam : George Hintzenweg
Position Category:Assessors
Position Type:Employee Regular

Who are LRQA?

LRQA stands for dedication to clients, market firsts, and deep expertise in risk management. We’ve grown to become a leading global assurance provider, bringing together outstanding expertise in certification, customised assurance, cybersecurity, inspection and training.

While we’re proud of our heritage, it’s who we are today that really matters, because that’s what shapes who we and our clients can become tomorrow. By staying true to our shared values and combining decades of collective experience, we support our clients in building a safer and more sustainable future.

LRQA currently operates across countries, has more than , colleagues, generates £m in revenue, and supports more than , clients across a diverse range of sectors and markets.

Key Responsibilities:

As a lead auditor and specialist in your field you independently or in a team verify management systems in the area of quality management mainly within the medical devices industry (ISO , ISO ). You will act as an expert and examine and assess the implementation of management systems at our clients all around the country. Your goal is to contribute to the improvement of the overall systems. The broadening and deepening of the collaboration with our relations is also a great aspect of your job. point of contact for your customers you maintain contact with them and / or ensure that their questions end up in the right place internally and are answered.

You will of course be supported by the various departments of our back office. 

The successful candidate should be able to demonstrate the following:

A minimum of a BSc degree, higher diploma or equivalent in a relevant science subject ( Mechanical Engineering or Electronics), as well as relevant postgraduate experience gained within the IVD industry, a clinical laboratory or medical research institution, is important and quality assurance experience would be an advantage At least years of working experience in the field of medical devices or relevant sectors preferably in various sectors. Wide knowledge of ISO & ISO Standards; Preferable successfully completed IRCA regd. Lead auditor training courses. Third-party auditing experience in the relevant sector. A good verbal and written knowledge of both Dutch and English language. Preparedness to travel when necessary to visit locations abroad Analytic insight and proactive attitude Qualification to other schemes ISO , ISO will be an added advantage.

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