Technical Writer
vor 2 Monaten
**Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.**
At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.
Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.
The **Technical Writer** for Beckman Coulter Diagnostics is responsible for writing, formating, producing, and revising technical documentation for existing product lines and new product development in our Content Management System (CMS). You will work as a member of project teams in an Agile development environment, and collaborate with Software Developers, Engineers, Technical Support, Project Managers, Product Managers, Regulatory Compliance, Quality Assurance, and other members of the team to gather information and obtain approval.
This position is part of the Technical Documentation department located in Munich and will be on site. This is a temporary position for 2 years.
If you thrive in a supporting role and want to work to build a world-class Technical Documentation organization—read on.
**In this role, you will have the opportunity to**:
- Ensure quality and technical accuracy of content and compliance with regulatory requirements
- Communicate project status and issues to Technical Publications Project Manager and/or Core Teams, Project Management, Analysts, Technical Writers, Coordinators, Management, and other stakeholders, as required
- Read, understand, and follow documentation and department procedures, including global procedures
- Ensure that skills are maintained on a continual basis to support Technical Publications activities and objectives, and participate in process improvement efforts
- Adhere to the company’s Style Guide, terminology guidelines, and relevant best-practice guidelines
- Define appropriate multimedia (such as 2D figures, 3D animation, photos, videos, screenshots) for accompanying written documentation
- Provide support for the Quality Assurance and Regulatory Affairs processes that the team adheres to
**The essential requirements of the job include**:_ _**
- Bachelor’s degree in Technical Communication, English, Journalism, or related field and relevant experience, especially in the medical device field.
- Excellent communication, writing, and grammar skills in the English language at the native-speaker level (German and or other language skills are a plus)
- Ability to create documentation for automated medical laboratory equipment (both hardware and software)
- Experience with or fundamental knowledge of CMSs, XML, and DITA
**It would be a plus if you also have experience in the following**:
- Experience with the following: SDL TriSoft, XMetal, Acrolinx, Illustrator, working in an Agile Development process
- Ability to prioritize work effectively and react appropriately in a dynamic work environment for completing deliverables on time
- Experience in, and know-how of, terminology management
- Ability to work and flourish in a diverse, multinational R&D environment
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
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