1 of 1 Temporary Validation Jobs in Cambridgeshire

the next generation of precision medicines. ** This is a 6 month fixed-term contract position ** The Technical Writer is responsible for creating, maintaining, and managing documentation related to the validation of Enterprise Resource Planning (ERP) and Manufacturing Resource Planning (MRP) software systems. This role requires a strong understanding of software validation principles, regulatory requirements, and ERP/MRP systems, as … well as exceptional writing and communication skills. The Technical Writer will collaborate with cross-functional teams, including IT, Quality Assurance, and business stakeholders, to ensure that all validation documentation is accurate, complete, and compliant. What youll be doing for us Validation Documentation: Develop, write, and revise validation documentation, including validation plans, protocols (IQ, OQ, PQ), summary reports, and traceability matrices. … and ensure the accuracy of documentation. Provide support and guidance to project teams on documentation requirements and best practices. Documentation Management: Manage the storage, organization, and version control of validation documentation. Ensure that all documentation is readily accessible, retrievable, and maintained in a controlled environment. Utilize document management systems to streamline the documentation process and ensure compliance. Compliance and Quality More ❯