Project Coordinator
Location: SwitzerlandSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Medical Devices and Pharmaceutical organization, based in Genf Switzerland.
They are one of the worlds leading pharmaceutical companies with multiple sites and offices spread around almost 200 countries. They have been around since the early 1700's and they are still growing.
ROLE DESCRIPTION
To support the Project Leader of a new E-Health platform in coordinating the project activities our client is looking for a Project Coordinator with work experience in technical documentation and project management, preferably in Medical Devices. In this position you will closely work with the Project leader to consult on for example Design History File maintenance or the project's schedule advancement.
RESPONSIBILITIES
- Maintenance of the Design History File with technical documentation.
- Maintenance of project’s schedule and administration of invoices, purchase orders, etc.
- Organization of project’s meetings and preparation of minutes.
- Coordination / preparation of project milestones (Design Reviews).
- Maintenance of the project risk registry and follow-up on mitigation actions.
REQUIREMENTS
-At least a minimum of 5 years working experience with Project Management
-Also at least 5 years of experience in Technical Documentation (Design History Files)
-A minimum of 6 years working experience in a regulated environment
-Excellent organizational skills
-Nice to have's: Software development experience in Medical Devices and experience with E-health platforms
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact .
