RA / QA Manager - Promising Medical Software
1 day left
- Full Time
If you would like to work for a medical device start-up company, then I have an interesting proposal for you as Regulatory Affairs and Quality Assurance Manager. This company develops ground-breaking medical software that will improve the situation for as well doctors as patients so you can play a part in this and build good quality and regulatory processes.
You will be part of a cross-functional team as the only RA and QA responsible person which means you will perform all the operational activities but also decide on the priorities and long-term strategy to make sure the goals are reached. This will give you a lot of variety and accountability which will make the days fly by.
You will report directly to the CEO so you will know very well where the company is going and what is happening at all times. This will also make the decisions and communication a lot faster so you see things moving forward.
- Master Degree in Life Sciences or Engineering or similar by experience
- Some years of experience in Quality Assurance and/or Regulatory Affairs for the medical devices, diagnostics or pharmaceutical industry
- Knowledge of MDR/IVDR
- Experience or affinity with software or IT is preferred
- Fluent level of English
If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Consulting website or my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.
NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech 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. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.
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