cmc technical writer

What if your expertise could contribute to work that ultimately makes a difference for patients? Are you looking for an environment where collaboration, expertise, and meaningful challenges come together? Would you value the opportunity to work alongside experienced life-science professionals and contribute to projects across the industry? YES? So let's...

Who is Sonar?Sonar is driving the future of agent-centric software development. As the leader in AI code verification and governance, we solve a critical problem: ensuring that software generated by AI-assisted developers or autonomous agents is reliable, secure, and maintainable.Integrating seamlessly with Claude Code, Codex, Cursor, GitHub Copilot, Gemini,...

The Technical Writer is responsible for creating, updating and maintaining Isovalent Enterprise Platform and Hypershield documentation as a whole, the main part of it being developer and user documentation. You will be at the forefront of our users' experience for both open-source Cilium and our enterprise offerings, making the most technically advanced...

​Join our Team!Hightech from Switzerland We are an internationally active technology company with locations in Switzerland and subsidiaries in the United States, Germany, France and India. Our interdisciplinary teams combine expertise in mechanical engineering, electrical engineering, software and information technology, working together to develop...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Technical Writer - PostgreSQL based in Switzerland. This is an opportunity to join a distributed open-source software team focused on PostgreSQL and related database technologies. You’ll own the creation of clear, accurate, and...

Hamilton Medical AG in Bonaduz, Switzerland, seeks a dedicated Team Lead for our information developers delivering end-user documentation for our devices and related products.You will lead a small team, collaborate with engineering, clinical input, and regulatory bodies, ensuring on-time, high-quality documentation. Requirements include proven end-user...

Cisco Systems, Inc. in Zürich is seeking an experienced Technical Writer to create, maintain, and improve enterprise documentation for Isovalent’s Cilium distribution and Hypershield.You will craft developer and user guides, reference manuals, and best practices to empower users across open-source and enterprise offerings. You will collaborate with...

Die Gesundheit der Menschen ist wichtig. SCHOTT Pharma entwickelt Lösungen, die weltweit sichere und einfach anzuwendende Medikamente gewährleisten. Ein Team von 4.700 Mitarbeitern aus über 60 Nationen trägt zur globalen Gesundheitsversorgung bei. Mit 17 Standorten weltweit ist das Unternehmen in Mainz ansässig, an der Frankfurter Börse gelistet und...

Randstad Switzerland recherche un rédacteur technique pour l'équipe Recherche & Développement afin de concevoir, organiser et diffuser une documentation technique multilingue.Vous rédigez et actualisez les notices et fiches techniques, structurez la documentation machines et coordonnez les traductions (anglais, allemand ou italien). Vous collaborerez...

The Technical Writer is responsible for creating, updating and maintaining Isovalent Enterprise Platform and Hypershield documentation as a whole, the main part of it being developer and user documentation. You will be at the forefront of our users' experience for both open-source Cilium and our enterprise offerings, making the most technically advanced...

SCHOTT AG in Sankt Gallen sucht einen Fachmann für technische Dokumentation, der eine Schlüsselrolle in der Erstellung und Pflege von Dokumentationen für Produkte übernimmt. In dieser Position arbeiten Sie eng mit Engineering R&D und externen Partnern, um sicherzustellen, dass alle Dokumentationen den relevanten Normen entsprechen.Die Stelle erfordert...

Sonar is seeking a Senior or Staff Technical Writer to own developer-facing content across the SonarQube product suite. You will work closely with engineers and PMs, in the same repos and PRs, shaping documentation as a discipline and maintaining high-quality examples and tutorials.You will craft guides, tutorials, and release notes, ensuring content remains...

Wir ermöglichen was unmöglich scheint. Denn bei SCHOTT wissen wir, dass gemeinsame Verantwortung, Erfahrung und enge Kollaboration bahnbrechende Lösungen hervorbringen. Als globaler Konzern für Materialtechnologie finden wir so neue Wege, eine bessere Zukunft zu gestalten – für unsere Partnerunternehmen, unsere KundInnen und unsere...

Stellenbeschreibung: Über uns Die Gesundheit der Menschen ist wichtig. SCHOTT Pharma entwickelt Lösungen, die weltweit sichere und einfach anzuwendende Medikamente gewährleisten. Ein Team von 4.700 Mitarbeitern aus über 60 Nationen trägt zur globalen Gesundheitsversorgung bei. Mit 17 Standorten weltweit ist das Unternehmen in Mainz ansässig, an der...

Novartis in Basel is seeking a Technical Project Leader (TPL) to drive a scientifically sound and business-driven CMC project strategy for TRD, including financial planning, risk assessments and contingency planning. The TPL will lead and support the CMC team, ensuring alignment with multiple departments and third parties, while promoting innovation and AI...

GRA CMC Manager to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, and lifecycle management. In this role, you will shape global CMC regulatory strategy, ensure compliant execution of submissions and changes, and partner with technical and regulatory teams worldwide. **Key...

Director, Regulatory Affairs CMC Europe Ready to lead the CMC regulatory strategy for novel small-molecule therapies in oncology? We’re partnering with an innovative biotechnology company that is advancing a portfolio of next-generation targeted oncology therapies. As the pipeline progresses towards global registrations, we’re looking for an experienced...

Position PurposePartnering closely with global and regional Global Regulatory Affairs colleagues, as well as Global Operations stakeholders, to address regulatory strategy challenges and deliver innovative, timely regulatory CMC solutions that meet evolving regulatory and compliance requirements. Supporting digital innovation, enabling capital project...

ppbThe Role What You Will Be Doing /b /p pThe Expert Medical Writer provides strategic, scientific, and operational leadership for the planning, authoring, and coordination of high-impact clinical and regulatory documents that support global marketing applications. In addition to hands‑on writing, the role serves as Programme Medical Writer for complex...

Responsibilities: Develop global regulatory CMC strategies for enterprise-wide CAPEX and compliance projects through collaboration with functional leaders in Global Regulatory Affairs CMC, Global Regulatory Affairs, R&D, Quality, Global Operations, and other business functions. Assess and facilitate the use of digital innovation for Global Regulatory...