Technical Writer

About the Role

Join a leading biotechnology company based in Dublin, engaged in pioneering solutions for areas with significant medical needs. The company seeks a Technical Writer on an initial 12-month contract to contribute to its mission of improving the lives of individuals affected by diseases.

Primary Responsibilities

• Develop, update, and maintain controlled Good Manufacturing Practice (GMP) documents such as procedures, records, and technical reports.
• Collaborate with manufacturing, engineering, and quality assurance teams to coordinate document revisions supporting operational changes and enhancements.
• Administer change requests related to documentation and ensure timely execution of required actions.
• Assist process investigations, improvement initiatives, and project tasks by providing accurate documentation and reviewing data.
• Oversee document workflows to spot and implement improvements in efficiency and regulatory compliance.

Qualifications and Experience

• Bachelor’s degree in Science, Engineering, or a related technical field.
• Previous work experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing sectors.
• Proven expertise in technical writing and document control within a GMP-regulated environment.
• Exceptional organizational skills with the ability to juggle multiple priorities effectively.
• Strong communication abilities and experience collaborating with diverse, cross-functional teams.