Senior Director Regulatory Affairs CMC - Zurich

+Job summary · 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 lead from the front both in strategy and team directive. · +QualificationsEducated to B ...

You will lead global Chemistry, Manufacturing and Controls (CMC) regulatory strategy for complex biological products.We value clear decision makers who build strong partnerships, solve problems with practical solutions, and support the growth of colleagues. · ...

Cytokinetics is a late-stage specialty cardiovascular biopharmaceutical company focused on discovering developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle per ...

· Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscl ...

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

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities, and supporting new MAAs. · ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities and supporting new MAAs. · Bachelor's degree in Life Sciences, Pharmacy, Engineering , or related field. · 5+ years' experience in EU Regu ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities and supporting new MAAs. · ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications lifecycle activities. · The role focuses on EMA submissions authority interactions post-authorisation maintenance for centrally authorised medicinal products. · Lead ...

Manage regulatory activities for assigned Daiichi Sankyo products in Switzerland. · ...

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, ...

We are seeking a strategic and visionary Senior Director Global Launch Lead to lead the global launch of empasiprubart in Multifocal Motor Neuropathy MMN currently in Phase 3.Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives ba ...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back.We are building a new kind of biotech company one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our busin ...

· Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our ...

We are seeking an experienced Regulatory Affairs Manager to join our team in Switzerland. The successful candidate will have significant working experience in Regulatory Affairs within the pharmaceutical industry, with emphasis on regulatory pre-submission and post-approval activ ...

We are united by a single purpose,to improve lives around the world through innovative medicines. · Manage regulatory activities for assigned Daiichi Sankyo products in Switzerland · ...

We are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. · Act as a senior regulatory expert with a focus on CMC · ...

Shape CMC regulatory strategy for complex biologics in a fast-growing biotech environment · For a fast-growing, internationally active biotech company focused on biosimilar development, we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workp ...

We are looking for an experienced Regulatory Affairs Manager for our complex and highly regulated environment. · We pride ourselves on our integrity intensity innovation and involvement. · The successful candidate will take their place within the engaged knowledgeable Thermo Fish ...

The Senior Director leads global regulatory policy and intelligence capability anticipating and shaping change into actionable strategies across R&D functions. This role is hybrid onsite and remote working with key responsibilities in strategic leadership team management policy a ...