Investing in People

Are you an experienced Technical Writer looking to make an impact in the medical field? Do you want to create clear, accurate documentation that supports both product development and user training for life-saving medical devices? Join a dynamic team and contribute to the success of cutting-edge medical products! Key Responsibilities: Develop comprehensive documentation for technical products, including user manuals, guides, and technical specifications. Collaborate with engineers, product developers, and other stakeholders to ensure accuracy and consistency. Edit and revise existing content for clarity, consistency, and compliance with standards. Ensure all documentation meets regulatory and compliance requirements. Requirements: Bachelor's degree in Biomedical Engineering, or a related field. At least 3 years of experience in technical writing within the medical device industry, including instructions for use, patient brochures etc. Excellent written communication skills and the ability to simplify complex concepts. Familiarity with regulatory standards for medical devices. Fluency in German and English.   If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.  

Instructional Designer (Digital Training) Location: Hamburg area (hybrid flexibility) Are you an innovative Instructional Designer with expertise in digital training media? Do you excel in Articulate Storyline, Adobe CC, and H5P to create engaging and high-quality digital learning experiences? Our client, a global leader in healthcare diagnostics, is renowned for its groundbreaking products and dedication to enhancing the healthcare journey. They’re currently seeking an International Instructional Designer to join their digital training team and make a significant impact in advanced e-learning development. Main responsibilities: Develop, design, and produce engaging digital training content for medical diagnostics and healthcare topics Create and integrate graphics, animations, videos, and interactive elements into training modules Lead digital training project management, from conceptualization to release, ensuring high-quality output Collaborate with international instructional design experts to refine and innovate training solutions Continually improve workflows to maintain and elevate the quality of training media produced What is required: Advanced skills in digital training development with expertise in web-based training using Articulate Storyline. Strong graphic design skills with Adobe Photoshop, Illustrator, and After Effects, along with basic video production and post-production experience. Solid experience in technical and scientific storytelling, with resourceful communication skills to collaborate effectively with SMEs. Experienced in planning and coordinating training media productions. Adaptable and quick learner, open to continuous skill growth and enthusiastic about contributing to an international, intercultural team. 3D design skills with tools like 3DS Max, Cinema 4D, or Blender would be an advantage. Fluency in English (written and spoken). Willingness to travel globally (up to 30%). What is offered: Assistance for relocation to the Hamburg area. Hybrid working model with 30 days of annual leave. Broad learning and development opportunities, including access to an on-site training campus. Christmas and holiday bonuses, childcare support, subsidized pension plan, company discounts, and canteen lunch subsidies. In-house gym, sports courses, massages, psychological support, and general health management services Public transport subsidy, bike leasing options, and free parking. If you enjoy leading your own projects, collaborating with subject-matter experts, and working within a dynamic, international team, this opportunity may be a perfect fit! Who Are Adaptive Life Science? Here at Adaptive Life Science, we provide specialised recruitment services to the Life Science sector, covering the Medical Device, Diagnostic, and Biotech industries globally. We are connected with the most innovative medical companies in the world, and are ready to support your career development with them. Why Apply With Us? Our services are 100% free to candidates, and our focus is helping you find your dream job that aligns with your career goals, technical skill set, and culture fit. We offer a range of services, including: Expert advice on your CV and cover letter Guidance on salary expectations Personalized interview preparation Connections to exclusive job opportunities Assistance in negotiating the best possible offers 50% of the CVs we send to clients are accepted Accepted or declined, either way we will provide you with feedback We believe in being your trusted advisor throughout your job search. We will take the stress out of the process by working around your schedule, and with your needs. Who Do Adaptive Work With? We offer a wide portfolio of over 150+ Life Science companies, from start-ups with impressive funding and innovative product development, mid-sized companies investing in R&D, all the way to market leaders with significant global presence. If you are interested in this role, please apply with your CV or contact Dominika Wyrwinska for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry. dominika.wyrwinska@adaptivelifescience.com #LI-DW1 #LI-Hybrid

Are you passionate about ensuring safety and quality?   Do you enjoy navigating regulatory standards and managing product compliance?   Join our innovative client and play a crucial role in ensuring their devices meet all regulatory requirements and safety standards.   This position is ideal for someone with an engineering background, with a solid understanding of regulatory requirements who thrives in a detail-oriented, cross-functional environment!   Key Responsibilities: Identify and interpret compliance standards for our products. Assess standard updates and determine necessary adjustments with relevant departments. Develop product specifications for new products based on industry standards. Oversee approvals and maintain certifications by collaborating with both internal teams and external authorities. Work closely with certification agencies (e.g., UL, TÜV) to meet industry requirements. Plan, coordinate, and conduct risk assessments for our medical devices (including electronic components and software). Support product development in defining and validating risk-reducing measures. Schedule and perform routine reviews of risk assessments.   Requirements: Bachelor's degree in Engineering e.g. Electrical Engineering or equivalent technical training with relevant professional experience. Familiarity with regulatory requirements for medical devices or electronic appliances. Excellent communicator and team player who enjoys interfacing between development and regulatory compliance. Fluency in German and English.   If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.