Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.As part of Danaher's Biotechnology segment, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.The Technical Writer for Cytiva is responsible for creating and updating technical, production, and quality documentation. This includes work instructions, labor times, equipment maintenance guidelines, product specifications, process flows, logistics procedures, safety protocols, and standard operating procedures. The role also involves revising internal documents for accuracy and presentation and developing style guides, templates, workflows, and trackers.This position is based on-site and is part of the Operations team in Pensacola, Florida. At Cytiva, our vision is to advance future therapeutics from discovery to delivery.In this role, you will have the opportunity to:
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 ISO9001, 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.
The essential requirements of the job include:
Bachelor’s degree in Technical Communication, Engineering, or a related field with 3-5 years of relevant work experience
Strong knowledge of content development cycles, documentation best practices, and tools
Experience in creating and managing style guides, document workflows, and version-tracking systems
It would be a plus if you also possess previous experience in:
Translating technical jargon into clear, concise language for a non-technical audience.
Working in the Pharmaceuticals or Medical Device industry
Experience with Veeva & Magic systems
The salary range for this role is $75k—$90k. This is the range that we, in good faith, believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range, and this range may be modified in the future.This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 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.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.
