Validation & Qualification Engineer
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 offer medicines, vitamins, cosmetics products and healthcare accessories that are offered through the pharmacy and hospitals. They develop, manufactures and market a wide range of prescription-free medicines and health products.
ROLE DESCRIPTION
In this role you will guide the staff with your opinion to buy the right new machines. You will make sure that the validation and qualification and maintenance is all up to date. In this role you will make sure the machines are valid based on the GMP guidelines. If you are driven to do the qualification and validation at a pharmaceutical company, then this is the job for you!
RESPONSIBILITIES
In the position you will be responsible for drawing up the validation file for equipment and software used for making, packaging or assessing pharmaceutical products. Drawing up a file with specifications for new machines. Next to that you are responsible for the following:
- Advice on buying new machines.
- Preparing a complete, correct and clear validation file
- Maintenance and follow-up of the Validation Master Plans with the aim to determine and implement the validation strategy.
- Monitor the planning and roll out in time for re-qualifications with the aim of evaluating the system on a regular basis throughout the system life cycle, whether it is still in conformity (GMP, procedures, ...).
REQUIREMENTS
- MSc with technical or IT specialty (or relevant experience)
- At least 1,5 years work experience
- Accurate, communicative, assertive, orderly and systematic
- Experience in project planning
- Speaking and writing Dutch and English fluently
- You have good communication skills and team player
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.
