Regulatory Writer

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...

**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...

**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 -...

**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...

**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...

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 people own their careers. Their ideas, big and small,...

**About the role**: As Product Quality Expert (PQE) you will report directly to the Head of Quality Compliance & Systems and be responsible for compliance/regulatory activities related to biologic products. The PQE is the representative for different responsibilities, including: Regulatory Compliance activities, Interaction with Authorities, External...

**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...

**Abbott **is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160...

General Description: The incumbent will report to the Head Commercial Quality Europe and will be responsible for supporting activities relating to BeiGene’s external GMP operations in Europe and as well as internal BeiGene GMP processes, ensuring procedures and systems are in place to support BeiGene’s commercial products. The incumbent will support...

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...

For our customer we are looking for a Principal Scientist (M/F/d) (Biomarker Development) to support us in Basel. **Responsibilities** - Develop and validate fit-for-purpose cellular biomarker solutions - Independently design, execute, and interpret experiments - Ensure high quality and timely delivery of internal and external results - Development and...

Are you ready to make a difference in the lives of patients suffering from severe rare conditions? Do you dream of being part of a biopharma leader that's rewriting the narrative of medical advancement? Look no further - To support our client growth, we are looking for an **Manufacturing Science and Technology (MSAT) expert.** **Role & Function** The MSAT...

Minimum qualifications: - Qualified Swiss lawyer (admitted to the bar) - Commercial experience as an attorney either in private practice or an in-house legal team. Preferred qualifications: - Experience in a private practice, government, or in-house as a legal IT specialist, or part of the media/technology legal team. - Experience in public speaking and...

For our client, a well-known pharmaceutical company in Basel, we are looking for a QA Associate (M/F/d). **Background** The Quality Assurance (QA) Associate ensures the integrity and compliance of GMP-relevant documents and batches. This role supports the timely release of GMP materials and adheres to cGMP standards within the Technical Research and...

Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application!At Sobi, each person brings their unique talents to work as a team and make a difference....

General Description:_ The position will report to the Director IMP Quality Europe and located in Basel, Switzerland. Core responsibilities to support day-to-day Quality operational activities supporting clinical studies in the EU region. Key responsibilities are assessment of product temperature excursions and review of clinical batch records ready for...

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,...

Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.Job DescriptionManufacturing...

Your Responsibilities: Something here caught your eye? Have a read. Maybe this is the one 800 million people! That’s the number of people we reach globally. Novartis is reimagining medicine to improve and extend people’s lives, and we are finding innovative ways to expand access to our latest treatments. As a member of the Digital Content & Campaigns...