Description
We have an urgent contract requirement for an experienced QA Specialist with good experience & understanding of Pharmacovigilance.Working for a Biotech facility acting as a contract manufacturing organisation with their own production facility & 'state of the art' technology, we are seeking a Senior QA Consultant with over 10yrs experience within QA Pharmacovigilance to carry out 6 audits - some of which will be based overseas including Asia.
You will be responsible for the entire process of audits including: Preparation, execution and reporting of audits as well as discussions with stakeholders & commercial agreement, contributing to ongoing procedures and strategic planning.
This a 6 month contract to be based in Holland with travel to client sites to carry out the audits.
3 x day week.
English language essential - any Dutch would be advantageous!