Technical Writer

2 weeks ago

Dublin, Ireland Ascend Project Management Full time

Ascend PM are hiring a Technical Writer to join our clients team, a pharmaceutical company based in West Dublin.This is a great Contract opportunity to join a growing team.Contact or email CV to to find out more.Overview:An experienced technical writer with a track record of developing user-friendly, comprehensive documentation.You will work within the Global Device Engineering department supporting the creation of medical device operator manuals and technical documents.Deliver content to support the delivery of state-of-the-art software solutions & GUI's.Key Responsibilities:Develop and edit medical device labelling content (e.g., user manual text and design, device labels) that is easy-to-read and understand by end users.Collaborate closely within a cross-functional team (with Regulatory Labelling, Quality, Clinical, Human Factors, Commercial, Engineering, Regulatory etc.) to optimize medical device labelling clarity and completeness.Translate technical jargon into user-friendly language to ensure documentation is accessible to a diverse audience.Extract relevant information from complex engineering documentation for use in clinical instructions, including working autonomously with limited direction.Understand regulatory requirements for medical device labelling, and develop labelling to meet these.Research new operator manuals, modifications to existing manuals, technical bulletins and other written material.Edit documentation written by others.Develop labeling for all medical devices and accessories.Stay up to date with product updates/changes, collaborating with development teams to ensure accurate and timely documentationWork within the defined company processes to ensure compliance.Conduct reviews and updates of existing documentation to reflect changes in software or hardware configurations.Support external language translations.Requirements:5+ plus years Technical Writing experience, preferably in a medical device environment.Excellent writing and editing skills, with a keen eye for detail and clarity.Demonstrated experience of producing medical device labelling content compliant with US and/or EU regulations and standards.Ideally experience using common technical writing tools (e.g., Adobe Creative Suite and MS Word, Excel, PowerPoint etc.).Knowledge of documentation quality management systems is desirable.Mastercontrol experience is an advantage.Excellent problem-solving methodology, using industry-accepted concepts and tools to solve complex problems in creative and effective ways.Comfort working in fast-paced, results-driven environments with tight timelines and frequent changes.#J-*****-Ljbffr

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