Quality Assurance 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 Pharmaceutical organization, based in Antwerpen Belgium.
They combine engineering, technology and port operations to offer worldwide, tailor-made solutions to the chemical and automotive industries, and to the consumer goods, electronics & retail sector. Active all over Europe, North America, South America and the Far East with a staff up to 13.000 employees.
ROLE DESCRIPTION
Are you ready for the next step in your career? Do you have passion for quality assurance? Do you follow the trends within this field? Within this role you will need to have a thorough knowledge of the European GDP regulations regarding storage, handling, transportation and fixed-term activities and also have a network that you can build on if certain questions are beyond your own knowledge-based domain? If you have these abilities this is the ideal job for you. This position will be at least for 6 months, with the possibility to extend.
RESPONSIBILITIES
As the Quality Assurance manager you take measures to prevent stolen or fake medicine enter the supply chain. Together with their clients you set up the management Standard Operating Procedures (SOP’s) and will keep the GDP licenses and any ISO licenses up to date. Next to that you will also be responsible for the following:
- provide training about GDP to our employees within the sector
- You guide the FAGG inspectors during the audits in the warehouses and operations (third party audits)
- You do the obligated self-inspections with the healthcare operations
- You got to follow CAPA plans
- You take decisions risk-based approach
- You have to make sure that all suppliers are certified
REQUIREMENTS
- Msc degree within the pharmaceutical/biotechnology industry
- Knowledge of ISO 9001 and ISO 13485 (certificate preference)
- You need to be interested in challenging time consuming projects
- You will have to be analytical
- You are a team player and communicatively very strong
- You need to be fluent in English Dutch and good with French
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
