SIRE Life Sciences®
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SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical, Biotechnology and Information Technology organisation, based in Noord-Brabant Netherlands.
The CompanyLeading biotechnology company in the field of human medicines.
Role DescriptionAssisting as a technical writer in a global project moving SaMD from Medical Device Directive to Medical Device Regulation.
ResponsibilitiesRewriting documents from MDD to MDR.
Requirements- Experience in regulated pharma environment
- Training in MDD to MDR with a recognized regulatory body
- Documentation skills
- Affinity with requirement documentation for Design History file
- Good in verbal and written English
Other information- Strong handling of time pressure
- Project management skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Sander Freeke.