| Position | Tecnical Writer |
| Posted | 16 Aug 2026 |
| Expired | 15 Sep 2026 |
| Company | Claran Consultants |
| Location | Cork | IE |
| Job Type | Full Time |
Latest job information from Claran Consultants for the position of Tecnical Writer. If the Tecnical Writer vacancy in Cork matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.
Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Claran Consultants for the position of Tecnical Writer below matches your qualifications.
A global biotechnology company is seeking a Technical Writer to join their team on an initial 12 month contract onsite. This role requires strong technical writing expertise with training coordination, thereby ensuring regulatory compliance, inspection readiness, and support personnel cross-training. The role requires demonstrated skills for initiative, self-motivation, outstanding organisational skills, and a proven ability to work independently. Key Responsibilities Technical Writing Lead, develop, and drive the ongoing enhancement of the documentation management strategy Produce high-quality, accurate documentation by applying data integrity and ALCOA principles, adhering to compliance best practices, and ensuring all materials are appropriate for their intended audience Serve as Subject Matter Expert (SME) for Veeva Quality Documents & Compliance Wire, offering guidance and support to colleagues in the use of these systems Draft, review, and approve BPDs, SOPs, technical protocols & reports, forms, work instructions, and other document types Collaborate closely with technical SMEs and teams to gain deep business and product knowledge for accurate documentation requirements Demonstrate excellent verbal and written communication skills to engage and motivate diverse audiences Propose and implement continuous improvements to the technical writing process, such as developing Advanced Templates Support Technical Writing activities across the site and collaborate with various departmental SMEs Manage the transition of documentation into Veeva Quality Documents and initiate Change Requests as necessary Support Global Training &/or Bus Ops with BcoE training development programs and materials, guides, and e-learning modules to address identified learning requirements Education and Experience (required): Third level qualification in a Science or an Engineering discipline, and/or extensive related proven experience in the required areas: technical document writing Skills: pharma science Engineering technical writing veeva TPBN1_IJ
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