TEAM HORIZON | Technical Writer | dublin

6 days ago


Dublin, Ireland TEAM HORIZON Full time

Team Horizon is seeking a Technical Writer for our client in Dublin. As a Technical writer you will be responsible for updating and creation of new technical procedures and SOPs for new equipment and equipment upgrades. Hybrid working available. Why you should apply: You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin. There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve peoples lives. Generous rates and flexible working hours. What you will be doing: Write and update technical documentation for Equipment Projects and Validation teams, including validation protocols, reports, and equipment specifications. Develop and maintain documentation for new equipment installations and equipment upgrades, ensuring all relevant procedures are clearly documented. Create and update Standard Operating Procedures (SOPs) for new equipment and equipment upgrades, ensuring documentation is accurate and meets regulatory requirements. Revise and maintain technical procedures to reflect changes in equipment functionality, process improvements, or new regulations.: Familiarize yourself with D2 file storage and collaboration repositories (or similar document management systems) for storing, sharing, and version-controlling documents. Ensure that all documentation is properly organized, stored, and accessible by relevant stakeholders in a structured, auditable manner.: Gain a thorough understanding of Oral Solid Dosage (OSD) manufacturing equipment, including tablet presses, granulators, blenders, and other related machinery. Document operating procedures, troubleshooting guides, and maintenance instructions for OSD equipment. Develop and update documentation for packaging equipment, including blister pack lines, bottle filling lines, sachet lines, and serialisation systems. Ensure that documentation for packaging equipment meets regulatory standards for serialization and traceability. Apply engineering and pharmaceutical knowledge to produce technical documentation that aligns with Good Manufacturing Practices (GMP). Ensure that documentation is suitable for a GMP environment, including validation reports, qualification protocols, and equipment calibration records. Develop and update documentation related to GMP equipment cleaning procedures, ensuring compliance with regulatory guidelines. Write and revise cleaning validation protocols and related documents, as well as create standard procedures for equipment and room cleaning in GMP environments. What you need to apply: Bachelors degree in a scientific or engineering discipline (e.g., Pharmaceutical Sciences, Engineering, Life Sciences). Technical writing certification or similar qualification is an advantage. Minimum of 3 years of experience as a technical writer, preferably in the pharmaceutical or engineering sector. Experience creating documentation for equipment validation, SOPs, and GMP compliance. Familiarity with manufacturing processes in pharmaceutical production, particularly OSD and packaging equipment, including serialization. Strong technical writing, editing, and proofreading skills with a focus on clarity, accuracy, and regulatory compliance. Knowledge of pharmaceutical and GMP standards and regulations (FDA, EMA, ICH). Proficiency in using document management systems (e.g., D2, Veeva, or similar) to store and organize documents. Familiarity with pharmaceutical equipment, including OSD manufacturing and packaging machinery (blister, bottle, sachet lines). Strong understanding of GMP equipment and cleaning procedures. Skills: OSD Technical Writing GMP Pharma



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