SIRE 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!
Our client is a professional Medical Devices organization, based in Switzerland.
The company is a global Medical Devices company, known for their high quality standards and their drive for innovation
Your main responsibility will be the maintenance/ improvement of the Quality Management System (QMS) according to ISO 9001 and ISO 13485. You will initiate CAPAs, lead in-and external audits and set up SOPs.
- Set up SOPs (with suppliers)
- Manage complaints
- Take part in internal and external audits
- Develop and maintain the QMS
- Report to the Director Quality Switzerland
- Good knowledge of ISO 13485
- Good knowledge of FDA 21 CFR 820
- Operating within all levels of the organization
- Technical education
- Fluent English, proper command of Italian is a big plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Matthias Kunkel.