Manager, Global Stability Technical Writer

**Stability and Sample Manager (M/F/d) - LIMS / GMP / German / English / Documentation** **Project**: For our client, a large pharmaceutical company based in Basel, we are looking for a **Stability and Sample Manager (M/F/d)** **Background**: We work with passion to improve the health and lives of patients. We show courage in our decisions and actions. And...

**The Role**: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners...

**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...

We are looking for our client, a pharmaceutical leader based near Neuchatel, a principal scientist stability for a one year contract (may be extended). Your responsibilities: You are responsible for stability product strategy and oversight of product stability programs for commercial small molecules Drug Substances and Drug Products Oral and Sterile: -...

**INTRODUCTION**: As a preferred supplier for Roche in Basel, we are looking for an individual as **Technical QA Manager**: - (contract for 1 year, with possible extension). The earliest start date is within 3 months. Remote/Homeoffice: on-site is required, home office upon discussion. **ASSIGNMENT DESCRIPTION**: - (general) IMP Quality Operations...

For our client, a well-known pharmaceutical company in Basel, we are looking for an Analytical Expert (M/F/d). **Background** We are at the forefront of innovative therapies with 14 Radio Ligand Therapy (RLT) projects in our rapidly expanding development pipeline. As part of our Global Technical R&D team, the Analytical Research & Development (ARD)...

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...

**Who is Aixial Group ?** Aixial Group, we are a CRO (Clinical Research Organization), specialized in Life Science. We work with laboratories to provide technical support on clinical projects from phases I to IV and post market. Since 2014, we have been part of the Alten family. We are developing our activities in Switzerland, France, Belgium, Czech...

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...

**Technical QA Manager** **Technical QA Manager (M/F/d) - GMP / Pharma / Qualification / Validation / CSV** **Projekt**: For our client, a big pharmaceutical company in Basel we are looking for Technical QA Manager (M/F/d). **Background**: **Tasks & Responsibilities**: - Running, maintaining and continuously improving Qualification/Validation activities...

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...

**The Role**: Reporting to the Sr. Director of Global Quality Control, the Manager, Global QC Change Controls (& Deviations), will be collaborating closely with Moderna’s network of QC Laboratories, internal and external (affiliated Contract Testing Organizations (CTOs)/Contract Manufacturing Organization (CMOs)), with the main following responsibilities...

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,...

**Project**: For our customer a big pharmaceutical company in Basel we are looking for a highly qualified **Technical QA Manager (M/F/d).** **Background**: The IMP Quality Operations Unit Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland...

**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, Novartis in Basel, we are looking for a reliable and motivated **Process...

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...

**Deputy Secretary General to the Financial Stability Board (FSB)** The FSB’s mission is to promote international financial stability; it does so by coordinating national financial authorities and international standard-setting bodies as they work toward developing strong regulatory, supervisory and other financial sector policies. The Deputy Secretary...

**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...

**Key Responsibilities/Scope of the Job** **Shared responsibilities**: - Act as analytical lead when appropriate for managing analytical projects under his/her responsibility - Cross functional interaction/collaboration within Sobi organization. - Interaction/collaboration with CDMOs/CLOs as required by the projects. - Act as a technical expert for...

**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...