Quality Consultant - QMS
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 and Pharmaceutical organization, based in Brussel Belgium.
Our client is one of the Top20 pharmaceutical and medical devices companies.
ROLE DESCRIPTION
In this project with a minimum duration of 4 months you will support our client with the harmonisation of multiple quality systems. Furthermore your key tasks will include the implementation of the ISO 13485: 2016 revision and supporting the client with quality issues, audits and general QA tasks.
RESPONSIBILITIES
- Support of key projects at our client top harmonize the quality management systems
- Implementing the 2016 revision of ISO 13485
- Take part in audits/ regulatory inspections
- CAPAs, Change Controls, Complaints, Documentation review and approval, ...
- Implementing regulatory requirements into lab environment
REQUIREMENTS
- QA experience as freelancer or consultant
- Good knowledge of relevant regulatory standards (ISO 13485:2016, 21 CFR 820, EMA, CLIA/CAP)
- Fluent in English
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.