N: HamiltonMedicalAG
Hamilton Medical is a dynamic, internationally successful medical device company headquartered in Bonaduz, Switzerland. At Hamilton Medical, we live for ventilation technology. Technology that helps caregivers improve the lives of their critically ill patients. We believe that innovation is essential to meet the demands of critical care.
To strengthen our multinational team, we are looking for motivated people in all areas of the company: from software developers to medical or healthcare professionals, from engineers to export specialists, from production workers to regulatory affairs specialists, and from project leaders to product managers.
Job Description:
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Lead and develop the team Technical Content and Information Design
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Promote positive employee morale within the organization by mentoring/empowering employees and facilitating development plans together with Head of Global Technical Support and Services
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Develop, design and maintain technical documentation, service manuals, support guides, company statements and process documentation in English language using available source documents, specifications and project information
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Initiate and conduct regular meetings with Product Management, Product Innovation and Design, Procuct Care and Quality Management to discuss documentation requirements for new product developments and changes to existing products and processes
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Communicate and drive compliance with policies and standards for the production of documents and publications
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Ensure that all process stakeholders (direct and partners) are trained to comply with all applicable policies and procedures as defined in the Hamilton Medical Quality Management
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Define and control deadlines and/or KPIs to ensure that all procedural and quality requirements are met
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Gather, correlate, and verify change or project-relevant information from various sources
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Report regularly on project status and other developments to Head of Global Technical Support and Services
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Participate in project teams
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International travel requirement up to 20%
Qualifications:
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Master's degree in biomedical engineering preferred or equivalent combination of education and experience
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More than 3 years of experience in leading technical expert teams with a focus on technical support documentation
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Profound experience with creation of technical documentation, service manuals and instrumental guidelines for biomedical devices in English language using available source documents, specifications and project documents
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Background with Intensive Care Unit procedures preferred, knowledge in mechanical ventilation an advantage
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Strong communication, interpersonal and negotiation skills and ability to influence cross-functional teams without formal authority
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Speak/write/read English and German (fluent or native)
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Ability to grasp and explain complex technical concepts through simplified text and graphics in a way that the target audience can understand and interpret the information correctly
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Excellent skills and knowledge in the use of documentation production programs such as Adobe InDesign, Illustrator, Photoshop, FrameMaker and Microsoft Office, experience with SCHEMA ST4 an advantage
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Experience with European medical device regulation (EU) 2017/745 as well as with American FDA laws and regulations an advantage
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Enthusiastic leader, driving high performance combined with a culture of accountability while providing an environment of appreciation and respect
Are you interested? Then please apply online by clicking on the "Apply" button. There you will also find our contact details for any queries.
Applications by post or e-mail can unfortunately not be considered.
