Technical Writer

Scope: Full-Time, Permanent EmploymentJob Title: Technical WriterIndustry: AviationResponsibilities:Create and maintain Aircraft Maintenance Manual (AMM) and Illustrated Parts Catalog (IPC) supplements for all ATA chapters in compliance with airworthiness standardsDevelop and maintain internal guidelines for technical documentation.Design and produce...

**About the role**: Takeda’s Neuchatel Manufacturing Sciences/Quality Compliance teams are looking for a highly motivated Technical Writer. The role is expected to have a solid understanding of regulatory guidelines as well as background of biopharma processes including related GMP requirements. **How you will contribute**: **Your mission** As Technical...

Genedata transforms data into intelligence with innovative software solutions that incorporate extensive biopharma R&D domain knowledge. Multinational biopharmaceutical organizations and cutting-edge biotechs around the globe rely on Genedata to digitalize and automate data-rich and complex R&D processes. From early discovery all the way to the clinic,...

**The Role**: In addition, the Global Stability Technical Writer will be responsible for supporting Global processes for harmonizing and integration of stability-related activities. Global Stability Technical Writer will also assist during HA Audits and will lead the governance of stability related processes and systems at Global level. **Here’s What...

**Marketing Content Writer (Cloud/DevOps) - Remote (EMEA)** **Description**: We’re seeking a Marketing Content Writer to join our global and fully remote team at amazee.io. You'll be crucial in creating engaging and informative technical content showcasing amazee.io's technological solutions, services, and industry expertise. You'll be responsible for...

500! The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority...

Genedata transforms data into intelligence with innovative software solutions that incorporate extensive biopharma R&D domain knowledge. Multinational biopharmaceutical organizations and cutting-edge biotechs around the globe rely on Genedata to digitalize and automate data-rich and complex R&D processes. From early discovery all the way to the clinic,...

ProClinical is partnering with a leading optical pharmaceutical organization in the search for a Technical Project Manager in Zurich. This is an exciting opportunity to join the IT and Digital Leadership Team. They are looking for someone to be responsible for the development of concepts and the implementation of technical projects. **Responsibilities**: -...

**Outlier helps the world’s most innovative companies improve their AI models by providing human feedback. **Are you an experienced Swiss Italian** writer who would like to lend your expertise to train AI models?** **About the opportunity**: - Outlier is looking for talented writers with fluency in Swiss Italian to help train generative artificial...

**About Idorsia Pharmaceuticals Ltd** Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core. Headquartered in Switzerland - a European biotech hub -...

Our Engineering Technical Documentation Team is looking for a strong writer to support us in delivering aircraft documentation (maintenance and operation manuals). Under supervision of the tutor and using templates and guidelines, you have the opportunity to gain professional experience in an interesting and exciting working environment. -...

500! The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority...

We're looking for an Intern who will play a crucial role in the future of our company. Our Intern. will be responsible for the public documentation at Auterion. You'll be collaborating closely with the engineering team, as well as providing our OEMs with documentation to build from. **Responsibilities and Duties** - Create, improve and update documentation...

Summary: Since 1967, Jet Aviation has been crafting flight in its smoothest form. From one hangar in Basel, Switzerland, to some 4,000 employees, and some 50 locations worldwide. Aircraft Management, Aircraft Sales, Charter, Completions, Defence, FBO, Fixed and Rotary Wing Maintenance, and Staffing. Behind every seamless Jet Aviation experience, is a team of...

Summary: Since 1967, Jet Aviation has been crafting flight in its smoothest form. From one hangar in Basel, Switzerland, to some 4,000 employees, and some 50 locations worldwide. Aircraft Management, Aircraft Sales, Charter, Completions, Defence, FBO, Fixed and Rotary Wing Maintenance, and Staffing. Behind every seamless Jet Aviation experience, is a team of...

Switzerland, Basel Switzerland, Monteggio Switzerland, Visp Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our...

VHR is hiring for our client who provides refurbishment, aircraft management, aviation consulting and maintenance services. This is an excellent opportunity for someone looking for a permanent position with growth opportunities.Job Description:Work in accordance with applicable procedure as per the Client's AC DOE, POE, MOE, CAME and other...

Hobson Prior are currently seeking a Medical Device Technical Expert - Human Factor to join a brilliant pharmaceutical establishment on a contract basis located in Basel. Our client is focused on offering novel solutions that acknowledge the developing requirements of people and communities. Please note that to be considered for this role you must have the...

EUMEDICA Pharmaceuticals AG is an independent and privately owned pharmaceutical company founded in 1986 in the heart of Basel, Switzerland.Our responsibility is to ensure continuity of access to patients and healthcare professionals to our unique and targeted therapeutic solutions portfolio.We focus on niche, severe pathologies, and therapeutic...

**EINFÜHRUNG**: Our profession and our passion "HR Management." Global Personal is an independent company of the Interiman Group SA with over 100 employees offering a complete range of human resources services at 21 locations in German-speaking Switzerland. For our client, an international orientated company in Basel, we are looking for a reliable and...