Regulatory Affairs & Quality & Safety Affairs Senior AssociateCzech Republic An exciting opportunity to join an innovative, dynamic and game-
changing team within a multinational healthcare company with a diverse portfolio. Must have a Minimum 2 years in regulatory affairs experience in industry Responsibilities Registration and maintenance of medicinal productsCommunication with local regulatory authoritiesEnsuring compliance with legislative requirements for all products of the companyCommunication with relevant state authoritiesQuality assurance and quality control of productsDevelopment and innovation of productsMandatory reports to state authorities and internal reportsPharmacovigilance Deputy LPPV(Local contact person for pharmacovigilanceDistribution and maintainence of GDP (Good distribution practice) Candidates that apply must be authorised to work in the EU and send me your up to date CV, along with your achievements and experiences outlined.
If you’re interested in this opportunity do not hesitate to contact me ASAP for this opportunity as a Senior Scientist of Upstream bioprocessing.
Ideally you can send me your CV with this relevant information : Salary starting expectations and your best achievements within your career to make you stand out from the other candidates and your notice period or earliest starting date to give you the greatest chance of successfully obtaining this opportunity.
EMAIL : sdiez barringtonjames.com
Phone number : (+44) 0 1293 776644
Mobile : (+44) 0 7513 257178