Quality Procedures Jobs in Prague

As a Quality Control Inspector youll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA the role of Operations is to deliver our industryleading services to our clients while ensuring that all the work is performed to the QIMA standard of quali More...

Role and ResponsibilitiesThe Quality Officer will support all audit activities within PrimeVigilance and will work with the Auditing team and Quality team s to ensure audits are delivered in line with PrimeVigilance and procedures and global regulations.The Quality Officer will perfor More...

As a Quality Control Inspector youll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA the role of Operations is to deliver our industryleading services to our clients while ensuring that all the work is performed to the QIMA standard of quali More...

The Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Inf More...

The Quality Management Officer is responsible for ensuring that Quality Events (QEs) and Corrective and Preventative Actions (CAPAs) are completed in accurate and timely fashion and are managed in compliance with global regulations legislation and PrimeVigilance requirements.Lead the More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

Job framework data:Work location: Canton St. GallenWorking Model: HybridEmployment Type: Full TimeHome office: 80%TasksManage projects focused on quality processes including areas such as First Article Inspection Incoming Inspection and InProcess Inspection.Act as the primary coordina More...

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Phys More...

The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk More...

This is an exciting opportuniy for a freelancer / consultant to join our team as a Person Responsible for Local Literature Screening at 0.5 FTE.By working with us you will have the opportunity to work in an international team.Main responsibilitiesPerforming local scientific literature More...

Providing support to other activities undertaken by the project team on behalf of the client andthe companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to):Processing Individual Case Safety Reports (ICSRs) fro More...

Providing support to other activities undertaken by the project team on behalf of the client andthe companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to):Processing Individual Case Safety Reports (ICSRs) fro More...

Providing support to other activities undertaken by the project team on behalf of the client andthe companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to):Processing Individual Case Safety Reports (ICSRs) fro More...

Providing support to other activities undertaken by the project team on behalf of the client andthe companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to):Processing Individual Case Safety Reports (ICSRs) fro More...

The Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf More...