Description
A global pharmaceutical organisation, based in the Mid-West Region of Ireland is looking for a Technical Writer for a contract role until the end of 2016.Essential Duties and Responsibilities include:
- Write, create, draft, edit, review and maintain documents for the Automation department.
- Performs Data verification for studies and reports.
- Ensure consistency of content, format, layouts of all related protocols and reports.
- Edit, standardise, or make changes to material prepared by other writers or establishment personnel.
- Assists in the review/approval process for protocols and reports through paper based or electronic systems.
- Writes, reviews, and maintains department standard operating procedures.
Experience:
- Proven experience in technical writing to support our Automation department
- Does need an understanding of automation but does not need extensive engineering background.
- Proficient in Microsoft applications such as Word, Excel, PowerPoint and Project.
- Experience in document systems would be beneficial
- Experience in GMP systems would be beneficia
- Resolves problems, identifies issues and determines system improvements
- Attend meetings relevant to assigned projects as needed.
Please apply now for more information!