Please refer to JobSuchmaschine in your application
QA Validation Specialist
SIRE 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!
Our client is a professional Biotechnology, Medical Devices and Pharmaceutical organization, based in Zürich Switzerland.
Our client is a healthcare company in central Switzerland
Supporting the Process Validation projects, making sure that activities are compliant with QMS and external guidelines (FDA & EU).
Facilitate risk assessment/FMEA process.
Review and approve validation plans and reports and lab manufacturing equipment qualification (IQ/OQ/PQ).
Perform QMS maintenance activities and implement quality improvement activities.
Provide GMP guidance.
University Degree in Scientific discipline.
5 years experience working in life sciences
Excellent knowledge of EU and USA legislation
Proven experience in process analysis and method validation and experience in risk management, six sigma tools and applied statistic methods.
Complete fluency in English language.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.