Auditor Medical Devices

2 maanden geleden

Rotterdam, Nederland LRQA Nederland B.V. Voltijd

Company: LRQA

Job ID:40121
Location:Rotterdam : George Hintzenweg 77
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 50 countries, has more than 2,500 colleagues, generates £315m in revenue, and supports more than 60,000 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 9001, ISO 13485).
  • 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 (e.g. 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 4 years of working experience in the field of medical devices or relevant sectors preferably in various sectors.
  • Wide knowledge of ISO 9001 & ISO 13485 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 e.g. ISO 14001, ISO45001 will be an added advantage.


Diversity and Inclusion at LRQA:

We are on a mission to be the place where we all want to work and we are passionate about embracing different perspectives because we understand the value this brings to our business, our clients and each other. We are all about creating a safer and more sustainable future and our inclusive culture is right at the heart of our business.

Together our employees make our communities better and we want you to be part of our diverse team

LRQA is a leading global assurance provider. The integrity and expertise we bring to our partnership with clients support their journey to a safer, more secure and more sustainable future. (Group entities).

Copyright © LRQA 2021. All rights reserved. Terms of use. Privacy Policy.

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