Associate Director, EUCAN Regulatory Lead - Zürich - Takeda

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. · Provide strategic, operational and tactical regulatory insight on pre-approval and post-approval activitiesHelp guide the organization on the appropriate filing strategy ...

+Job summary · Takeda is seeking an Associate Director to join its Oncology team as the EUCAN Regulatory Lead.+ResponsibilitiesDefines regional progressive regulatory strategies. · Communicates regulatory strategies. · ...

Takeda is seeking an Associate Director to join its Oncology team as the EUCAN Regulatory Lead. This role involves partnering with senior regulatory leads to define regional regulatory strategies for late-phase oncology assets. ...

We are currently seeking an Associate Director to join Takeda's Oncology team as the EUCAN Regulatory Lead. · This role is crucial for our growing oncology portfolio, where you will partner with the assigned asset senior regulatory lead to define and lead regional strategies with ...

Job DescriptionContributes to the development of regulatory strategy for assigned clinical trials in Europe & Canada (EUCAN) and Growth & Emerging Markets (GEM) regions. · Demonstrates Takeda leadership behaviors. · ...

This position contributes to the development of regulatory strategy for assigned clinical trials in Europe & Canada (EUCAN) and Growth & Emerging Markets (GEM) regions. · Develops the operational implementation plan for clinical trial applications (CTAs) in EUCAN and GEM regions ...

As Regional Regulatory Lead (RRL), you will be responsible for defining and driving the regional regulatory strategy and its execution for a diverse portfolio of Immunoglobulin products across APAC, LATAM, and Partner Business markets. · Working closely with Local Regulatory Repr ...

As Regional Regulatory Lead (RRL), you will be responsible for defining and driving the regional regulatory strategy and its execution for a diverse portfolio of Immunoglobulin products across APAC, LATAM, and Partner Business markets. · ...

We are seeking a Policy and Regulatory Content Lead to help strengthen Hitachi Energy's strategic positioning as a global technology leader in the energy sector. · Craft and execute a thought leadership strategy that showcases Hitachi Energy's technology and innovation leadership ...

We are looking for an accomplished professional to join our Regulatory Reporting team in our Zug office. The team leads the firm-wide regulatory reporting platform, acting as center of expertise. · ResponsibilitiesEnd-to-end ownership: Oversee the production and sign-off of regul ...

We are looking for an accomplished professional to join our Regulatory Reporting team in our Zug office.The team leads the firm-wide regulatory reporting platform, acting as center of expertise. · End-to-end ownership: Oversee the production and sign-off of regulatory reports, en ...

We are seeking an experienced Global Regulatory Affairs Lead (m/f/d) to join our Technology (R&D) team in Lucerne. · Develop and implement global regulatory strategies for new and existing products. · Maintain a centralized regulatory database with 100% accuracy and accessibility ...

We are looking for an accomplished professional to join our Regulatory Reporting team in our Zug office. · The team leads the firm-wide regulatory reporting platform, · acting as center of expertise. In this role, · you will take full ownership of preparation, oversight, · and st ...

GC International AG is a global leader in dental care and oral health seeking an experienced Global Regulatory Affairs Lead to join their Technology team in Lucerne. · ...

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 profess ...

This role plays a pivotal part in shaping and executing the global Regulatory Chemistry Manufacturing and Controls strategy for Biogen's small molecule portfolio.You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delive ...

+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 Biogen's small molecule portfolio.++Shaping and executing the g ...

+Als Business Development Manager entwickelst du unser Kundenportfolio aktiv ausbaust bestehende Partnerschaften strategisch weiterentwickelst und skaliert unser Service Offering in einem stark wachsenden Markt. · ++ Aufbau Ausbau und aktive Steuerung von Kundenbeziehungen im ...

The role of Regulatory Affairs Manager involves supporting the development and registration of vaccine candidates in Europe. This includes managing regulatory projects, ensuring compliance with regulations, and collaborating with global counterparts. · ...

+Join Takeda as Director, Global Regulatory Affairs CMC Marketed Products Development (MPD) Lead... · +Independently manage regulatory submissions for assigned compounds... · ...

Blackfield Associates are supporting a renowned pharmaceutical client based in Switzerland who have a requirement for a Senior Director Regulatory Affairs CMC to join their team and lead from the front both in strategy and team directive. · Manage regulatory submissions for assig ...