| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | London |
| Education | Not Mentioned |
| Salary | 300.00 - 375.00 per day |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract , full-time |
*Pharmacovigilance Quality Specialist - Global Pharma - 12-month rolling contract* My client is a Global Pharmaceutical company and they have a position available for a Quality Specialist to join their team for a 12-month initial contract.Primary Responsibilities:- Supports establishment of GxP Global Procedural Documents to ensure a consistent GxP process landscape for standards and processes and procedures related to clinical development and safety/pharmacovigilance which meet internal and external standards of regulatorycompliance, as well as industry best practices and interpretations. - Builds and maintains strong relationships with key business stakeholders and ensures that the department is providing an efficient, effective and compliant process landscape to the functions. - In close collaboration with supported functional areas and key business stakeholders, identifies needs for process standardisation, regulatory compliance direction and areas for improvement. - Ensures that business partner expectations for Procedural Document strategy, materials and deployment are met.- Ensures, in collaboration with business partners, that Global Procedural Documents in the GxP process landscape are up-to-date and regulatory compliant versus current Clinical and safety/pharmacovigilance international regulations.- Collaborates with a network of subject matter experts (SMEs) across the functional areas, supporting the Global Procedural Documents development. - Contributes to the departments Standards, Systems & Processes Governance Team to set strategies and achieve the long-term goals and objectives. - Supports internal process improvement projects.In order to apply for the Pharmacovigilance Quality Specialist contract, you should possess experience of working in the Pharmaceutical Industry in the field of pharmacovigilance with strong knowledge of Good Pharmacovigilance Practices. You will possess excellenttechnical writing skills with the ability to produce clear, concise documentation and communications, alongside, good presentation and analytical skills. Experience of GxP , GCP and / or GVP knowledge is needed.Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on .
Keyskills :
GCPPharmaceuticalPharmacovigilanceQualityContractsystemsregulationsGXPGVP