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

WHO WE ARE:

Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services RD, production, packaging, and delivery processes—globally—with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx’s partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company’s experience and comprehensive suite of capabilities and solutions, visit www.catalyx.ai.

REQUIREMENTS:

• 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.

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.