Build your career on Magnet.me
Create a profile and receive smart job recommendations based on your liked jobs.
As a Product Reviewer – SaMD (Technical Documentation Reviewer), you play an essential role in assessing the safety, performance and compliance of innovative medical devices according to the MDR. Kiwa has a focus on Software as a Medical Device (SaMD) and AI-enabled technologies for innovative SME’s. Your expertise contributes directly to bring safe and innovative devices to the patient.
Overview
In this position, you independently perform technical documentation assessments and support certification process. Kiwa supports a hybrid working environment: after your start-up period, you will work one day per week from our office in Woerden, while the remaining days can be performed from home. You will occasionally travel within Europe for unannounced audits as a technical expert. Regular audits are performed by our lead auditors (other role).
Key Responsibilities
Responsibilities
You are an experienced reviewer with strong analytical skills.
Requirements
What we offer
About Kiwa
Kiwa is a global leader in TIC services with a mission to improve safety, quality and sustainability.
Team Description
You will join a supportive and improvement minded team with high expertise and different nationalities. We stay close to our SME customers while keeping our impartiality and independency.
SHV originated in 1896 in the Netherlands from a merger between a number of large coal trading companies. After the decline of coal as the primary source of energy, halfway through the twentieth century, SHV decided to diversify and move into other business areas.
SHV is present in 56 countries on all continents and employs approximately 60,000 people. For more information, please visit: www.shv.nl
View what's on offer:
Change language to: Dutch
This page is optimised for people from the Netherlands. View the version optimised for people from the UK.