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.It requires diligence, attention to detail, good communication skills and the ability to work as part of a team. This is a hybrid role requiring 3 days per week on-site.Job 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.Job Requirements:Five (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.Leadership Characteristics: Making Complex DecisionsComplex problem solving and decision-making based upon the available data.Leverages personal experienceOpen and collaborative styleDecisive and comfortable working within research & development projects.Communicating EffectivelyWrites and presents effectivelyAdjusts to fit the audience and gets the message acrossManaging Diverse RelationshipsEffective at building strong cross functional relationships with the key stakeholdersCommunicates up and down appropriately and effectivelyAbility to develop relationships and collaborate with multiple internal / external stakeholder groups.Acting with IntegrityIs a person of high character; is consistent and acts in line with a clear and visible set of values and beliefs; deals and talks straight; walks his/her talk; is direct and truthful but at the same time can keep confidences