Technical Writer

QCS Staffing; Dublin; On-site; EUR 45,000 - 65,000; Full time

Job summary

QCS Staffing is seeking a Technical Writer in Ireland, Dublin, for a 12-month contract with a globally recognised biotech client.

You will create, revise and maintain GMP documentation, coordinate with manufacturing, engineering and quality teams, and support investigations with precise data reviews to ensure compliance and efficiency.

Qualifications

• Degree in Science or Engineering or related technical discipline.
• Experience in regulated GMP environments preferred.
• Strong technical writing and document management skills.

Responsibilities

• Create, revise and maintain controlled GMP documentation (procedures, records, technical reports).
• Coordinate document updates with manufacturing, engineering and quality teams.
• Manage documentation-related change requests and ensure timely actions.
• Support investigations, process improvements and project activities through accurate documentation and data review.
• Monitor document workflows and identify opportunities to improve efficiency and compliance.

Skills

Strong written communication

Cross-functional collaboration

Education

Degree qualification in Science, Engineering or a related technical discipline

Job description

Technical Writer – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Technical Writer. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to support them on their global mission to better the lives of those affected by disease and illness.

What You’ll Deliver

• Create, revise and maintain controlled GMP documentation, including procedures, records and technical reports.
• Coordinate document updates with manufacturing, engineering and quality teams to support operational changes and improvement initiatives.
• Manage documentation-related change requests and ensure timely completion of associated actions.
• Support investigations, process improvements and project activities through accurate documentation and data review.
• Monitor document workflows and identify opportunities to improve efficiency and compliance.

Experience required

• Degree qualification in Science, Engineering or a related technical discipline.
• Previous experience within a pharmaceutical, biotechnology, medical device or other regulated manufacturing environment.
• Strong technical writing and document management experience within a GMP setting.
• Excellent organisational skills with the ability to manage multiple priorities simultaneously.
• Strong communication skills and experience working with cross-functional stakeholders.