Principle CMC Expert - Zug

This role provides the opportunity to be an independent SME across Drug Product manufacturing and development within a cross-functional Biologics environment. · The position reports to the Head of CMC/SCM and carries end-to-end accountability for technical transfers, Clinical and ...

This role provides senior technical leadership across Drug Product manufacturing and development within a cross-functional biosimilars environment. Lead end-to-end technical transfers to and between CDMOs. · Act as senior SME for Drug Product manufacturing and formulation develop ...

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 · ...

We are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus.Shape CMC regulatory strategy for complex biologics in a fast-growing biotech environment · A key role within a growing Regulatory Affairs team contributing to multiple development programs an ...

For a fast-growing internationally active biotech company we are looking for a Senior Expert Regulatory Affairs with strong CMC focus. · ...

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 ...

+Job Summary · Cytokinetics is seeking a Director of Regulatory Affairs-CMC to lead regulatory support for assigned programs and ensure sound regulatory planning and tactical implementation of US and international regulatory submission strategies. · +ResponsibilitiesFormulate CMC ...

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 ...

The Director/Senior Director, Global Regulatory Policy & Intelligence is a strategic leader responsible for building and executing a global regulatory policy and intelligence capability that anticipates, shapes, and translates regulatory change into actionable strategies across R ...

The Senior Director is a strategic leader responsible for building and executing a global regulatory policy and intelligence capability that anticipates, shapes, and translates regulatory change into actionable strategies across R&D, · regulatory submissions, product lifecycle an ...

The Director/Senior Director, Global Regulatory Policy & Intelligence is a strategic leader responsible for building and executing a global regulatory policy and intelligence capability that anticipates, shapes, and translates regulatory change into actionable strategies across R ...

The Sr. Manager of Drug Substance (DS) Process Development CMC will lead tech transfer, process qualification and validation at contract drug substance manufacturing sites. · ...

Opportunity awaits those up to the challenge of developing transformative therapies across a broad range of debilitating diseases. · As part of the Process development team, the Sr. Manager of Drug Substance (DS) Process Development CMC (Chemistry Manufacturing & Controls) will ...

We are seeking a highly skilled Early Clinical Development Medical Director- Oncology to join our dynamic Oncology Research and Development team. · The successful candidate will create a strong link between Clinical Development and Pre-clinical/ Discovery teams to improve forward ...

GSK is seeking a Clinical Development Medical Director- Oncology to join our dynamic Oncology Research and Development team. · Medical degree from accredited medical school · Completion of a clinical residency program · ...

GSK Oncology Early Clinical Development is seeking a highly skilled and motivated Early Clinical Development Medical Director- Oncology. · ...

GSK Oncology Clinical Development is seeking a highly skilled and motivated Clinical Development Medical Director- Oncology. · ...

+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 ...

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

Join us as our Global Manufacturing Sciences CMC Lead and drive high-impact, high-visibility CMC projects for innovative biologics in a dynamic global environment. · You will provide technical and strategic leadership for Chemistry, Manufacturing and Controls (CMC) of one or more ...