Develop and update technical documents, including work instructions, equipment maintenance guides, calibration procedures, quality specifications, process flows, logistics procedures, safety protocols, SOPs, and training materials. Review and Revise Documentation: Enhance existing documents to clarify and comply with Cytiva standards and the life sciences industry best practices. Support Training and Compliance: Create clear training content for technicians and operators, ensuring adherence to ISO 9001, ISO 14001, PSM, and Cytiva QMS requirements. Create Style Guides and Visual Content: Implement style guides and templates for consistency, using visuals to enhance comprehension and engagement. Document Processes and Track Updates: Maintain process flows for manufacturing and operations, using tools to manage document versions and ensure alignment with changes. Who you are:Bachelors degree in Technical Communication, Engineering, Business or a related field with 2 years of relevant wor...Technical Writer, Technical, Writer, Manufacturing, Business Services