Validation engineer (Quality)
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 Waals-Brabant Belgium.
They are a chemical company who develop and produce active pharmaceutical ingredients as well as advanced intermediates for the pharmaceutical, cosmetic and green chemistry industries. They have been supporting their customers for a long time in the scale-up and development of their products, with an emphasis on safety requirements and high quality standards.
ROLE DESCRIPTION
You will become responsible for the compliance of validation activities and ensure site procedures for qualification and validation remain aligned with current authorities. Do you like to communicate in a constructive way to induce quality mindset and do you have affinities for administrative work? Then this is the job for you!
RESPONSIBILITIES
You are responsible for the coordination of validation and qualification activities. You perform the qualification of IT systems and ensure these are adequately documented. next to that you will be responsible for the following:
- You ensure the compliance of qualification and validation documentation
- You take part to the Quality audits performed by Health Authorities and Customers and to the definition and implementation of corrective actions
- You act as contact person for the different internal departments such as IT, Quality Control team and production
- You participate to the maintenance of the Quality system
REQUIREMENTS
- MSc or Ph.D. in pharmacy, engineering, IT, chemistry or biochemistry
- At least 2–5 years of relevant experience in the field of qualification or validation activities in a GMP environment
- Excellent knowledge of French and English
- You are IT minded and you have good knowledge of statistical process control tools
- You are able to tackle complex problems with logical mind and you deliver insightful, practical solutions in a continuous improvement mindset
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.
