This position is no longer open for applications

• Perform in-process, final product testing and stability analysis of drug substance and drug products.
• To support the development, optimisation and validation of analytical test methods, either in-house or in collaboration with external service providers.
• Support the technical transfer of Zoetis analytical test methods to and from Zoetis Tullamore site.
• Write test method and validation protocols, SOPs and other quality system documentation to allow the execution of the analysis in a GMP environment. This will include trending data, monitoring Out of Specifications and participating in laboratory investigations.
• Work closely with the process development group to support the development of a robust manufacturing process and transfer to the GMP facility.
• Work closely with specialist contract testing service providers to ensure excellent collaboration is maintained throughout the project.
• Support raw material testing when required for GMP manufacture
• Support the identification of equipment requirements and work with vendors to ensure execution of all deliverables, including equipment qualification and validation.
• Participate in Quality and Safety regulatory audits.

Internal candidate identified