Biopharmaceutical Technical Documentation Specialist
A challenging and rewarding contract opportunity is available for a skilled biopharmaceutical technical documentation specialist to join our team.
The role involves providing high-quality, accurate documentation applying technical writing principles and best practices in a biopharmaceutical company based in Cork.
About the Job
* Lead, develop, and implement process-related documentation management strategies.
* Produce high-quality, accurate documentation.
* Perform technical writing, transition of documents to Veeva System, and necessary editing.
* Create, manage, and maintain track changes, documentation repositories.
* Act as the Subject Matter Expert (SME) for these repositories.
* Closely collaborate with SMEs and teams to gain an in-depth understanding of the business and product.
* Evaluate and ensure accuracy and consistency of technical documentation.
* Suggest and implement continuous improvement to the technical writing process and toolset.
Requirements
* Bachelor's or Master's degree in a Science or Engineering discipline.
* Approximately 5 years of related proven experience in technical document writing.
* Stamp 1G or Stamp 4 visa (Applicants interested in contracting opportunities within the pharmaceutical sector in Ireland).