QA/QC Coordinator/Manager
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.
The company is a family business, which has grown into a Belgian market leader and specialist in the processes and services for textile management, sterilisation of medical instruments and logistics for the health sector. They are an innovative and flexible service provider where you will end up in a growing company, where values such as commitment, quality, sustainability are highly valued.
ROLE DESCRIPTION
As the right hand of the QA / QC manager, you will be closely involved in all quality aspects that characterises their services and this in accordance with the vision and mission of the organisation and the latest legislation.
RESPONSIBILITIES
Together with the QA / QC manager you form the central point of contact for QA / QC for the Central Sterilisation activities, the lab activities, the production of medical devices.
You will monitor the quality, the procedures and are also involved in the further development of the quality policy, given the business strategy.
You take an active role in concluding quality agreements and technical agreements with suppliers & customers.
You establish procedures, coordinate them with all parties involved and you ensure correct implementation and application.
You are responsible for following up and adjusting the quality for various internal and external contacts.
REQUIREMENTS
A Master in Life Sciences with a big plus in Pharmaceuticals
At least 3 years of experience in QA/QC with at least 1 year in Medical Devices
Knowledge of ISO 13485 & ISO 9001
Fluency in English and either Dutch or French (or Both)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.
