Quality Consultant - Product Safety
Location: BelgiumSIRE 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 organization, based in Limburg Belgium.
Our client is a developing Medical Devices company in Belgium specialised on the Healthcare industry.
ROLE DESCRIPTION
As consultant you will be responsible for performing the gap analyiss betweent the IEC60601 2.2 and 60601 3.0 directives and help the company implement the new standards.
RESPONSIBILITIES
- Performing the required gap analysis
- Consult the Quality department on results
- Responsible for development of new and revision of existing design controls, ensuring compliance with the quality system
REQUIREMENTS
- Good knowledge of MDD & ISO norms
- English fluent
- Ability to work 2-3 months on location
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Krems.
