Technical Writer

Uniting Holding; Cork; On-site; EUR 40,000 - 60,000; Full time

Job summary

A leading biopharma company is seeking a Technical Writer to support documentation at their site in Cork, Ireland. The candidate will create technical documents, ensure compliance with standards, and collaborate with experts. Applicants should possess a strong technical background, ideally with a PhD and experience in regulated industries. This role offers growth opportunities and a comprehensive benefits package.

Benefits

Total Rewards package

Professional growth opportunities

Support for Critical Skills Visa applications

Qualifications

• Strong technical background with industry experience.
• Proven track record in biopharma or life sciences documentation.
• Ability to prioritize workload and adapt to project demands.

Responsibilities

• Create and maintain various technical documents.
• Translate complex information into user-friendly documents.
• Collaborate with subject matter experts while managing projects.

Skills

Technical documentation

Attention to detail

Communication skills

Independent work

Education

PhD in relevant field

Tools

Veeva

Job description

Overview

Catalyx is seeking a Technical Writer to join our team and work on our customer site in Cork.

The Role

You will support the preparation of documentation across technical, quality, and operational functions. The right candidate will have a strong technical background who can work independently to produce accurate and compliant documents.

Responsibilities

• Create, edit, and maintain a wide variety of documentation including SOPs, safety and equipment procedures, maintenance guides, technical reports, and operational excellence procedures.
• Translate complex technical and scientific information into clear, concise, and user-friendly documents.
• Collaborate with subject matter experts while managing documentation projects independently.
• Ensure all documents meet regulatory, quality, and GMP standards.
• Work within electronic document management systems, particularly Veeva (experience desirable, training can be provided).
• Provide flexible support to align with global teams and project needs.

Qualifications

• Strong technical background, ideally with a PhD and relevant industry experience.
• Proven track record of producing technical documentation in biopharma, life sciences, or related regulated industries.
• Experience with technical transfers, technical reporting, or scientific documentation.
• Excellent written and verbal communication skills with strong attention to detail.
• Familiarity with Veeva or similar document management systems (desirable).
• Ability to prioritise workload, work independently, and adapt to changing project demands.

Why Join Catalyx?

At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities.

Equal Opportunity

Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone.

At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates.