Cmc Technical Writer

**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...

**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...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

GRANITE BIO is a recently established biotechnology company in the Ridgeline Discovery incubator located in Basel (Switzerland). Based on fundamental research over the last two decades, GRANITE BIO’s differentiated approach is to impact central disease biology nodes to transform inflammatory, autoimmune and fibrotic conditions. The lead therapeutic...

Regulatory Affairs Manager CMC For our client in Basel, we are looking for RA CMC Manager who will be responsible for global CMC submission activities for assigned projects. **Responsibilities**: - Identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical...

766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, there is more we can do to help improve and extend people’s lives - In Global Regulatory Affairs CMC, our work starts when a compound goes into clinical trials. Novartis has a unique and promising portfolio. All of these innovative projects are aimed at making a...

CMC Chemist **Responsibilities**: - You will be part of a team of process research, scale-up & supply chemists, purification and analytical sciences experts - Support a diverse portfolio of small molecule, peptides and nucleic acid discovery projects. - Develop synthetic routes for small molecules suitable for early toxicological and clinical phase I...

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,...

**Technical Project & Product Lead - Drug Product (Parenteral/Combination Product) - 5759 ADA** Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for a **Technical Project & Product Lead - Drug...

Proclinical are recruiting for a Regulatory Technical Manager for a pharmaceutical organisation. This role is on a contract basis and is located in Basel. *** **Responsibilities**: - Accountable for preparation and upkeep of CMC documentation in internal document management systems and assist with associate actions. - Handle regulatory changes throughout...

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...

**ALTOGEN** is a Swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices. With several years of experience, technical expertise and project coordination, we support our partners throughout all areas of the product life cycles. We surround ourselves with junior to expert...

**Technical Project & Product Lead - Drug Product (Oral Dosage) - 5752 ADA** Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for a **Technical Project & Product Lead - Drug Product (Oral...

Outlier helps the world’s most innovative companies improve their AI models by providing human feedback. Are you an experienced Swiss French 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 French to help train generative artificial intelligence...

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 intelligence...

**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...

A Swiss private bank specialising in wealth and asset management is looking to hire a senior Avaloq developer in Basel, Switzerland.The successful candidate will be a seasoned software engineer with profound know-how of all relevant technological aspects of the Avaloq stack (Avaloq Script, PL/SQL, Oracle SQL, Task Engine, Report Writer, Object Model,...

The Director - Vaccine Technical Operations: - Oversee and guide technical operations at internal and external manufacturing sites to ensure stable and cost effective commercial supply - Lead technical aspects of network development projects, process validation implementation, raw materials and components management - Represent Technical Operations on the...