Vacant job

Do you have an interest in technology, structure, and clear communication – and want to work in a global Life Science environment where documentation truly makes a difference? Then this could be the assignment for you!

For our client, a leading international company in Life Science, we are now looking for technical writers for consulting assignments in Uppsala. You will have the opportunity to work in a highly competent team responsible for customer-facing user documentation in areas such as chromatography, filtration, cell therapy, medical technology, and process equipment.

In the role of Technical Writer, you will be a key person in the creation, updating, and management of technical documentation for the client's products. The work is carried out in close collaboration with cross-functional teams in areas such as R&D, product management, regulatory, and manufacturing.

Examples of tasks:

• Create, edit, review, and publish user documentation for digital and printed formats
• Ensure that documentation adheres to company standards, brand guidelines, and legal and regulatory requirements
• Develop new technical documentation and update existing materials (text and illustrations)
• Collaborate cross-functionally with product management, R&D, regulatory functions, and manufacturing
• Plan and estimate time requirements and report status in documentation work
• Maintain documentation databases and inform relevant stakeholders about updates
• Contribute to the development and improvement of tools and platforms for documentation production

The assignment is a full-time consulting position, initially for 1 year with the possibility of extension, located on-site in Uppsala. The start is planned for March 1, 2026, preferably earlier.

WHAT WE ARE LOOKING FOR

Requirements for the position:

• Master's degree (MSc) in molecular biology, biotechnology, or a related field, or a bachelor's degree (BSc) with relevant experience
• At least 2 years of experience in structured technical or scientific writing
• Experience working with user manuals, instructions, or validation documentation
• Excellent command of English, both spoken and written

Meritorious:

• Experience with SDL Tridion or other XML-based CMS
• Knowledge of Adobe InDesign, Photoshop, and Illustrator
• Basic knowledge of HTML/CSS
• Experience with GMP, SOPs, or regulatory documentation
• Familiarity with Cytiva's products or similar Life Science equipment
• Experience with CAD tools or video editing

To thrive in this role, we see that you are communicative, structured, and meticulous, with an eye for detail and quality. You are accustomed to working against deadlines, thrive in a dynamic environment, and find it easy to collaborate with various competencies in global teams. You work independently but also appreciate close collaboration with others.

Does this sound like something for you? Apply for the position today – we only accept applications until January 16. Here you have the chance to develop in technical writing within a global company whose products contribute to improving people's lives.