Regulatory Standards Specialist
Location: NetherlandsSIRE® 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 organisation, based in Noord-Holland Netherlands.
- help DE answer our unsolved regulatory and business opportunity validation questions
- For example: Can we sell this product online? What needs to be done to sell that
product online?
- come up with a way that helps us drive eCommerce sales from a regulatory perspective
- deliver a way to move forward with our approach to sell medical devices/equipment online from a regulatory point of view
- support the prework for product onboarding of MATC (e.g. Efficia/SureSign/AED), X-Ray and Ultrasound equipment from a regulatory point of view
- understand German healthcare regulations in general
- have knowledge on digital sales of healthcare products
- have a general overview on eCommerce processes
- know about the requirements for selling DXR (StrlSchV - Radiation Protection Ordinance, etc.)
- ability to work from Hamburg, Germany office for 3 days a week in first month. Going forward, location can be flexible to Amsterdam office or Hamburg
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Hiariej.
Role Description
- Business development from a Q&R perspective: help validate and unlock new portfolio opportunities for eCommerce- help DE answer our unsolved regulatory and business opportunity validation questions
- For example: Can we sell this product online? What needs to be done to sell that
product online?
- come up with a way that helps us drive eCommerce sales from a regulatory perspective
- deliver a way to move forward with our approach to sell medical devices/equipment online from a regulatory point of view
- support the prework for product onboarding of MATC (e.g. Efficia/SureSign/AED), X-Ray and Ultrasound equipment from a regulatory point of view
Requirements
must have items:- understand German healthcare regulations in general
- have knowledge on digital sales of healthcare products
- have a general overview on eCommerce processes
- know about the requirements for selling DXR (StrlSchV - Radiation Protection Ordinance, etc.)
- ability to work from Hamburg, Germany office for 3 days a week in first month. Going forward, location can be flexible to Amsterdam office or Hamburg
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Hiariej.
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