Regulatory affairs Contract IVDR specialist.

Consultant with IVDR experience Swedish company

Are you an experienced Regulatory affairs professional with experience from working with IVDR?

Looking to expand on your experience with this field and continue your freelance career?

My client is a world renowned company in Medical devices and in particular IVD products.

They have been in this field since over 50 years and have been innovating their products ever since.

This would be a 6 month contract for 1,0 FTE, although this is negotiable for example if you have at least 0,6 FTE available that would be ok and the contract would go on for a longer period.

The work would mostly be done remotely but some visits on site in Gothenburg would be necessary for certain approval and sign of certain documents.

Work tasks:

The work will mainly consist of updating their regulatory documents and aiding them with the new regulations so that all their products follow their guidelines.

Requirements:

• Experience with IVDR
• Experience with MDR
• At least 5 years experience in Regulatory affairs
• Bachelors degree in life science or similar.
• Fluent in Swedish and English
• Having worked with IVD Devices previously.

Contact info

If this sounds right for you then send me your CV as the interviews are starting soon.

K.Danielsson@nonstopconsulting.com

+46 850 927 950 internal extension is 8118

if this does not sound like the opportunity for you, but you are a professional within the pharmaceutical, medical device or biotech industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry..