Medical Devices Contract Worksheet Approver

at

SGS

Antwerpen, Belgium
Full Time
10mo ago

Company Description

At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors’, people who can connect our diversity to our services. To each other. And this way, enrich our business.

SGS is the world’s leading inspection, verification, testing and certification company. We’re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to more almost 100 000 colleagues worldwide, with more than 1750 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.

Job Description

We are currently looking for a Medical Devices Contract Worksheets Approver (CWS Approver) for the SGS Notified Body 1639 in Antwerp.

The main responsibilities will be to review the customer's Medical Device Contract Worksheets (CWS) and to build the case for acceptance or rejection of the requested service maintaining the integrity of SGS.

In your role as a CWS Approver you review and approve Medical Device Contract Worksheets and associated documents to ensure they meet the requirements and matchs our Notified Body’s scope and capabilities. In addition, you will approve allocation of audit team competencies and establish lists of potential auditors based on procedures.

As such you ensure all Notified Body procedures have been complied with and the appropriate documentation duly completed.

Other responsibilities in your role are:

  • Ensuring the master service agreement, i.e. the contact between the client and the notified body, is finalized and signed.
  • Maintain you understanding the Medical Device Regulation by practice and in-house training.

Qualifications

For this position we are looking for someone with an academic or technical qualification such as Engineering, Sciences, Biomedical sciences. Our new colleague is organized, efficient and methodical in approach, with high attention to detail. He/she has demonstrated high level of interpersonal skills with the proven ability to communicate and influence effectively at all levels. Experience with medical devices (products) is a plus but not a must. You will be coached and trained in your general knowledge of business principles and operating practices (commercial awareness). You have a good knowledge in use of MS Office and are fluent in English and preferably in Dutch (any other EU language is an asset).

 

Additional Information

Do you want to be part of this?

We are looking forward to hearing from you! Send us your story and your resume via the apply button and maybe you will soon join us. For further information, please don’t hesitate to mail to [email protected]

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