Be part of something altogether life-changing!
 Being at the vanguard of developing novel approaches to improve human health is what it means to work at Cytiva. 
Our amazing clients work on projects that have the potential to save lives, from basic biology research to the creation of novel vaccines, medications, and cell and gene treatments. 
You will be able to constantly better both yourself and us at Cytiva by working on important challenges with people who genuinely care about each other, our clients, and their patients.
 With associates in more than 40 countries, Cytiva is a place where learning opportunities abound every day, enabling you to advance your career and broaden your skill set over time. 
We combine committed technological know-how and talent to create the next wave of game-changing medicines as a part of Danaher's Biotechnology division.
 For products created and maintained at Cytiva, the Senior Technical Writer is in charge of creating and managing user manuals that are intended for the company's customers in a style and manner that complies with corporate guidelines. 
This is a hybrid function that will be a part of the Technical Documentation group (TechDoc) in Uppsala. 
Our goal at Cytiva is to progress pharmaceuticals from discovery to market release. 
In this role, you will have the opportunity to:
 Complete end-user documentation assignments, such as updating preexisting technical documentation or creating new technical documentation for new product development (NPD). Determine the time needed to do assignments, plan it out, and give regular reports on your progress. 
To guarantee completeness, accuracy, validity, and clarity of information for digital and/or print production in accordance with corporate standards for style, branding, and quality, legal guidelines, and regulatory requirements, write, edit, review, proofread, approve, process translations, and publish end-user documentation. 
Collaborate with other departments (like project management, manufacturing, regulatory, product management, and research and development) to produce new documents on schedule and under budget, as well as to maintain current documents.
 For more complex projects with several deliverables, manage writer activity and update stakeholders on progress. 
Serve as a technical writer's mentor. 
Give technical writers advice on strategic choices pertaining to tools, documentation strategy, design, and content. Serve as the Technical Writers' point of contact for escalated project issues. exchange of knowledge, providing the team with technical writing assistance, organising techniques, and product domain knowledge. Specify procedures and guidelines. 
Contribute to the development and deployment of new platforms and tools for the effective creation and upkeep of user documentation. 
Encourage ongoing advancements. 
The essential requirements of the job include: 
An MSc degree in biology, chemistry, molecular biology, or a related discipline is preferred; alternatively, a BSc in science with at least four years of relevant professional experience is acceptable. 
Several years of more responsible experience producing, editing, and creating technical documentation for users, ideally in a medical device or life science setting. 
Proficient in both technical and information mapping English, as well as excellent communication abilities. Strong communication abilities both in writing and speaking; expertise in organising and reorganising documents; ability to create original technical writing; experience editing the work of others. 
familiarity collaborating with stakeholders and cross-functional teams. familiarity with Cytiva goods, especially with consumables (such as filters, columns, ELISA kit, resins, single-use, and cell culture media), medical equipment, and/or cell therapy items. experience using publishing tools like Adobe InDesign, Photoshop, and Illustrator as well as content management systems like SDL Tridion or other XML-based systems. 
It would be a plus if you also possess previous experience in: 
Outstanding interpersonal, communication, and organisational abilities. Detailed and methodical, with the capacity to set priorities and exercise initiative. 
Proven capacity to work on several projects concurrently, pursue tasks through to completion, be results-driven, problem-solving, and self-motivated. At Cytiva, we're committed to creating a workforce that is better and more sustainable. 
We are dedicated to delivering fulfilling jobs regardless of the work arrangement and acknowledge the advantages of flexible, hybrid working arrangements for qualified roles. 
This job qualifies for a hybrid work schedule, which allows you to work some hours remotely from home and some hours at the company's above-mentioned location. 
Your interview team will tell you more details about this hybrid work arrangement. 
Examine the challenges and flexibility that come with working for Cytiva. 
At Danaher, we combine science, technology, and operational skills to expedite the use of science and technology of tomorrow in practical applications.
 We collaborate with clients all over the world to help them overcome their most difficult problems by designing solutions that truly harness the power of science. 
Our international teams are setting the standard in the fields of biotechnology, diagnostics, life sciences, and other fields. 
To learn more, go to www.danaher.com. At Danaher, we embrace diversity and the presence of both apparent and subtle differences and similarities among our employees, in our workplace, and in the markets we service. These varied characteristics allow our associates, customers, and shareholders to give distinct and varied opinions.