Clinical supplies quality specialist

PpFor one of our clients, an international pharmaceutical company, we are seeking a bClinical Supplies Quality Specialist. /b /p h3General Information /h3 ul libEnd Date: /b /li libHome office: /b possible /li libWorking hours: /b Standard /li /ul h3About the work /h3 pThe Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs for usage in clinical studies. The team is responsible from release of clinical and commercial drugs, incoming label stock and primary packaging components to release of clinical finished good. /p p3 time per week the day starts at 9 with a team meeting to discuss ongoing jobs to be released (batch). During a day, the person will work on releases. /p h3Tasks Responsibilities /h3 ul liReview and release of incoming label stock /li liReview, and release of clinical finished goods, including review of the printed and applied label /li liGMP review of the batch record and review of the regulatory filings and the final release /li /ul h3Requirements /h3 ul liUniversity degree (bachelor or higher) /li libDeep understanding of working in GMP regulated environment /b /li lib2-3 years’ experience in regulated environment /b /li liPrevious experience in a similar role is highly appreciated /li libEnglish C1 mandatory, German is nice to have /b /li /ul pSounds interesting? Apply now – we’re looking forward to receiving your applications! /p /p #J-18808-Ljbffr