Opportunity exists to take on a key role as a Documentation Specialist in the biopharmaceutical industry. This challenging position involves developing and implementing process documentation management strategies.
About the Job
As a Documentation Specialist, you will be responsible for producing high-quality, accurate technical documentation applying best practices. Your duties will include performing technical writing, transitioning documents to Veeva System and editing. Additionally, you will manage documentation repositories and collaborate with teams to gain understanding of business and product.
Responsibilities
* Develop and implement process documentation management strategies
* Produce high-quality, accurate technical documentation applying best practices
* Perform technical writing, transition documents to Veeva System and editing
* Manage documentation repositories and collaborate with teams to gain understanding of business and product
* Ensure accuracy, consistency and compliance of technical documentation
You will work closely with colleagues as Subject Matter Expert (SME) on Controlled Document Systems and Veeva Quality Documents, providing support and guidance. You will also draft, review and approve SOPs, BPDs, Forms, Protocols, Reports, WI and other document types. Collaborate across departments and perform documentation transitions to Veeva Quality Documents. Manage Compliance Wire activities and administer training events within Business Center of Excellence.
Requirements
* Bachelor's or Master's degree in Science or Engineering discipline
* 5 years related experience in technical document writing
* Stamp 1G or Stamp 4 visa eligibility to work in Ireland without visa sponsorship