This role will focus on writing and validating technical documentation for the manufacturing process. As a Technical Writer, you will be responsible for generating protocols, reports, and other documents related to Cleaning Validation in a Pharmaceutical organization based in Ireland.
Key Responsibilities
* Write and review technical documents such as SIP protocols, validation reports, and deviation documentation.
* Analyze data from study runs to assess the impact of deviations on cleaning processes.
The ideal candidate should have experience in QA validation activities, including execution and approval of protocols. Additionally, they should possess strong administrative skills with exposure to GDP regulations.