Site Lead MDR EU
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 Pharmaceutical and Medical Devices organisation, based in Zuid-Holland Netherlands.
- Development and execution of Site project plan
- Site reporting at CSS Core Team level and reporting at Site Leadership Level
- Planning of EU MDR required deliverables for next wave (2020 and beyond)
- 5+ years of experience within regulated environment like Medical Devices or Pharma (FMCG or other highly regulated industry could be considered)
- Excellent Project Management skills
- Fluent in English (oral and written), Dutch is a plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.
The Company
This site develops and produces high-quality breast implants that find their application in plastic surgery all over the world.Role Description
Within this role you will be responsible for defining the plant scope. Develop and execute project plans and plan for the next wave of EU MDR required deliverables from 2020 and beyond. Leading the EU MDR implementation within this site.Responsibilities
- Defining plant scope and secure resources- Development and execution of Site project plan
- Site reporting at CSS Core Team level and reporting at Site Leadership Level
- Planning of EU MDR required deliverables for next wave (2020 and beyond)
Requirements
- BSc degree or higher- 5+ years of experience within regulated environment like Medical Devices or Pharma (FMCG or other highly regulated industry could be considered)
- Excellent Project Management skills
- Fluent in English (oral and written), Dutch is a plus
Other information
Full time preferred, 32 hours discussable. Ability to be on-site at least 3 - 4 days a week).Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
