Documentation Specialist

2 weeks ago


Cork, Cork, Ireland beBeeWriter Full time €60,000 - €80,000

At Catalyx, we are committed to attracting the best global talent. We are seeking a Technical Writer to join our team and support the preparation of documentation across technical, quality, and operational functions.The ideal candidate will have a strong technical background who can work independently to produce accurate and compliant documents. They will be responsible for creating, editing, and maintaining a wide variety of documentation including SOPs, safety and equipment procedures, maintenance guides, technical reports, and operational excellence procedures.The successful candidate will also translate complex technical and scientific information into clear, concise, and user-friendly documents. They will collaborate with subject matter experts while managing documentation projects independently.They will ensure that all documents meet regulatory, quality, and GMP standards. They will also work within electronic document management systems, particularly Veeva (experience desirable, training can be provided).The role requires a proven track record of producing technical documentation in biopharma, life sciences, or related regulated industries. The ideal candidate will have excellent written and verbal communication skills with strong attention to detail.They will be able to prioritize their workload, work independently, and adapt to changing project demands. They will also be flexible in providing support to align with global teams and project needs.At Catalyx, we understand that our people are our greatest asset. For this reason, we take care of them. The team benefits from a Total Rewards package, which includes great personal benefits and professional growth opportunities.We are 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.Seniority level: Mid-SeniorEmployment type: Full-timeJob function: Quality Assurance and ManufacturingIndustries: Pharmaceutical Manufacturing, Biotechnology Research, Manufacturing



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