Regulatory Submissions Jobs in Switzerland

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

As a Principal Medical Writer you will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions to ensure clarity credibility and consistency of clinical information throughout submission packages and clinica...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

Role SummaryAs the Global Compliance lead you will build up and lead the global program compliance & validation teams ensuring the compliance of the IT solutions being implemented in the domains of manufacturing warehouse & laboratories. You will coordinate cross-functional teams to ensure the solut...

Noema Pharma is a biotech company developing groundbreaking therapies to address the most disabling symptoms in orphan conditions of the brain and nervous system. Noemas research and development is focused on understanding and meeting patient needs using our novel therapies.TasksThe Head of Clinical...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Noema is developing a late-stage portfolio of oral small molecule therapeutics with well-characterized mechanisms and distinct features that offer unique therapeutic advantages for neurological and other disorders. The Company is advancing three programs in parallel across orphan and large-market in...

OverviewMonte Rosa Therapeutics (MRT) seeks to recruit an Associate Director/ Director Drug Product CMC to play a key role in advancing our drug product development programs from early-stage development through commercialization. The successful candidate will join the CMC group supporting Monte Rosa...

Job Description: As a Regulatory Affairs Manager you will be responsible for ensuring compliance with regulatory requirements related to the development approval and marketing of pharmaceutical medical device or other healthcare products. You will work closely with cross-functional teams to navigate...

About Us ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development manufacture and testing of tomorrows medicines. We support our clients in developing differentiated stable usable and...

About This Role As Associate Director Regulatory CMC Small Molecule Lead you will play a pivotal role in shaping and executing the global Regulatory Chemistry Manufacturing and Controls (RegCMC) strategy for Biogens small molecule portfolio. You will be responsible for leading cross-functional regul...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Compa...

We are looking for... ....a highly motivated Principal DMPK Scientist/DMPK Lead for our Development department. Your tasksContribute as Core Project Team member for selected projectsResponsible for DMPK in vivo efficacy and pharmacology activities and strate...

Small Molecules Basel SwitzerlandAbout BioVersysBioVersys is a Swiss clinical-stage biotech company dedicated to the development of innovative antibacterial therapies addressing the global crisis of antimicrobial resistance. With two small molecule assets in clinical development and a strong scient...

The Amazon Web Services Healthcare and Life Sciences (HCLS) Professional Services (ProServe) team is seeking an experienced Clinical ProServe Cloud Architect (PCA) to join our team in this role youll work directly with pharmaceutical and life sciences customers including senior technology and busin...

Job Description SummaryLocation: Basel Switzerland Working Model: #LI-Hybrid Hybrid (12 days per month on-site)Alternate Location: London (The Westworks) United KingdomWorking model(s): #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles of our London office)#LI-Remote Remote (if...

The Global Product Safety Scientist (GPSS) is responsible for providing safety scientific expertise and works with the Global Product Safety Science Lead (GPSSL) to develop and implement the Safety Science strategy for assigned Sobi products. The GPSS works collaboratively together with the GPSSL an...