Scientific / Technical Writer

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,...

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals._ **Deviation Writer**: **Job Summary**: The Deviation 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...

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 standards.Develop and maintain internal guidelines for technical documentation.Design and produce...

**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 Pharma company in Basel, we are looking for a reliable...

**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...

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. **Discover Impactful Work**: The Deviation Writer (M/F/d) will...

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. **Discover Impactful Work**: The Deviation Writer (M/F/d) will...

For our customer located in Basel/Switzerland we are currently looking for a**:Scientific/Medical/Narrative Writer **(M/F/d)** - **Pay rate range (given by client)**: 42,81 - 48,16 CHF/h **Tasks & Responsibilities** - Implementing bioinformatics data visualizations. **Must Haves** - Education: B.S., M.S. in computer science, software engineering, or...

**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...

**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 -...

**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 -...

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,...

We are a full-service medical communications agency and a publishing house with medical journals like the healthbook TIMES Oncology Hematology, the healthbook TIMES Das Schweizer Ärztejournal/Le Journal des Médecins Suisses as well as several healthbook CONGRESS Highlights, covering the latest insights from annual congresses like the ASCO, EHA, ASH, EULAR,...

We are a full-service medical communications agency and a publishing house with medical journals like the _healthbook TIMES Oncology Hematology_, the _healthbook TIMES Das Schweizer Ärztejournal/Le Journal des Médecins Suisses_ as well as several _healthbook CONGRESS Highlights_, covering the latest insights from annual congresses like the ASCO, EHA, ASH,...

**Job Title**: Medical Writer (Oncology) 12-month contract **Reports to (Title)**: VP Clinical Development Oncology **Location**: Europe **Direct Reports**: No **Department**: Clinical Development The Hengrui ex-China organization drives the development and commercialization of the Hengrui innovative medicines portfolio for the US, Europe and Japan. Our...

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...

500! The number of regulatory documents we authored last year. As a Regulatory Writer you will write and review high quality clinical and safety documentation for submission to regulatory authorities. **Location**: Basel, Switzerland #LI-Hybrid **Your responsibilities**: Your responsibilities include, but are not limited to: - To author and review high...

**Customer Service Representative II** **(externer Titel: Junior KundendienstmitarbeiterIn Labor)** Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life...

Stratpharma, an innovative Dermatology company, is offering a 2-month summer internship opportunity in Scientific Document Management. This internship is a chance for individuals passionate about the field of dermatology to gain hands-on experience in an exciting and rapidly growing company. The selected intern will be involved in various tasks related to...