Quality Assurance Officer GMP
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 Pharmaceutical organization, based in Flandre Orientale Belgium.
The client is an international client with multiple sites all over the world. The site in Gent is a manufacturing site providing production and process development services to pharmaceutical companies around the world.
ROLE DESCRIPTION
In this role you will be responsible for the QMS and support the clients activities in securing patient’s safety. You will be closely involved in the further development and maintenance of the Global Management System over the different sites of the network, in close collaboration with all internal stakeholders.
RESPONSIBILITIES
- GMP compliance
- Perform audits & self-inspections
- Provide support to the Global Distribution team for ongoing operations and projects deployment
- Provide training in the field of Quality
- Identify gaps or non-compliances in the data base and remediate
- Collect compliance indicating data, review and identify relevant signals
- Manage monitoring activity
- Download, review and archive data
REQUIREMENTS
- A degree in Chemistry or the Life Sciences ,
- Preferably with 2 years’ experience in a Quality environment in the pharmaceutical industry
- Knowledge of GMP
- Excellent writing and strong communication skills in English and Dutch. Any other language is an asset.
- A high level of self-motivation is necessary.
- Ability to perform audits, internally and externally
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
