Technical Writer

Job Description

Do you have experience in Technical Writing within the Pharmaceutical, Medical Device or Biotechnology industry and at least 2 years experience in a Quality or Validation background?

Then I have a very exciting Technical Writer opportunity that I am currently working on at the moment located in Limerick for one of Ireland's leading Biotechnology companies.

This is a 12 month hourly rate contract that offers a competitive salary.

Experience in the Pharmaceutical, Med Device or Biotechnology industry with a background in Quality & Validation is essential.

Key Responsibilities

• Support drafting and authoring of investigations, deviations, CAPAs and Change Control records in conjunction with various departments.
• Provide support & guidance on the content and structure of system records
• Experience in assessment of CIP/SIP issues during study runs and closeout of deviations
• Engage in the creation, review, authorship, and enhancement of templates & reports for data collection.
• Work together with other experts to guarantee the accuracy and quality of records.
• Coordinate the execution of activities to meet delivery timelines.
• Cooperate with Technical Owners to understand key critical information to support effective completion of technical records

Experience and Qualifications

• Bachelor's Degree in a relevant field
• 2 years of relevant industry experience
• Experience in writing and approving deviations
• Experience in Technical writing for continuous assessment

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.