Regulatory Affairs Cmc Senior Manager

**Summary**: **About the Role**: **Major accountabilities**: - Formulate, lead and drive global CMC regulatory strategy with a focus on innovation, balancing business benefit with regulatory compliance for XXX modality projects/products. - Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for...

**Summary**: **About the Role**: **Major accountabilities**: - Formulate and lead global CMC regulatory strategy with a focus on innovation, balancing business benefit with regulatory compliance. - Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products. - Identify the...

Summary:About the Role:Major accountabilities: Formulate and lead global CMC regulatory strategy with a focus on innovation, balancing business benefit with regulatory compliance. Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products. Identify the required documentation...

**Summary**: **About the Role**: **Major accountabilities**: - Formulate, lead and drive global CMC regulatory strategy for XXX modality pro-jects/products drawing on substantial regulatory expertise with a focus on innovation, maxim-izing the business benefit balanced with regulatory risks and compliance. - Identify the required documentation and any...

Summary:About the Role:Major accountabilities: Formulate, lead and drive global CMC regulatory strategy for XXX modality projects/products drawing on substantial regulatory expertise with a focus on innovation, maximizing the business benefit balanced with regulatory risks and compliance. Identify the required documentation and any content, quality and/or...

**RA CMC Associate Director (M/F/d) - Biosimilars, Novartis, Schaftenau, Austria** 583! That is the total number of projects and products on our Global Regulatory Affairs CMC project list. All of these innovative projects are aimed at making a difference in patients’ lives and we need your support. - As a member of our Global Regulatory Affairs CMC team,...

**Summary**: As Senior QA Compliance Expert you will support, facilitate and drive on-site regulatory CMC related launch and post-approval activities (post-approval changes, transfers, remediation, divestment, pruning and due diligence) of the Campus products to ensure timely supply to the markets in compliance with current regulatory obligations and...

Regulatory Affairs Associate (m/w/d) - 8! This is the number of biosimilars for which Sandoz has already received a marketing authorization, and that already provided increased access to life-saving medicines to patients worldwide while further biosimilars are under development. - As a Regulatory Affairs Associate (M/F/d) you contribute to bringing new...

Vollzeit - Langkampfen **Bezahlung**: Gehalt je nach Qualifikation und Erfahrung ab € 3.600; - brutto pro Monat **Ab**: 2023-02-20 **Balmung Medical Handel GmbH** - Webseite +43 (0) 5332 25400 Balmung Medical Handel ist ein datenfokussiertes Handelsunternehmen für Medizinprodukte, in welchem die Kundenzufriedenheit im Mittelpunkt steht. Unser...

Regulatory Affairs Associate (m/w/d) 8 This is the number of biosimilars for which Sandoz has already received a marketing authorization, and that already provided increased access to lifesaving medicines to patients worldwide while further biosimilars are under development. As a Regulatory Affairs Associate (M/F/d) you contribute to bringing new biosimilars...

**Summary**: **About the Role**: **Major accountabilities**: - You will support the global Medical Device & Precision Medicine regulatory strategy with a focus on innovation, maximizing business benefit balanced with regulatory compliance. - Lead, support and implement all global Regulatory Affairs Medical Device (RA MD) submission activities for assigned...

**Summary**: **About the Role**: **Major accountabilities**: - You will support the global Medical Device & Precision Medicine regulatory strategy with a focus on innovation, maximizing business benefit balanced with regulatory compliance. - Lead, support and implement all global Regulatory Affairs Medical Device (RA MD) submission activities for assigned...

Summary:About the Role:Major accountabilities: You will support the global Medical Device & Precision Medicine regulatory strategy with a focus on innovation, maximizing business benefit balanced with regulatory compliance. Lead, support and implement all global Regulatory Affairs Medical Device (RA MD) submission activities for assigned projects/products,...

394430BR **Technical Project Leader - f/m/d**: Austria **About the role** At Novartis, we don't just create life-changing medicines. We build partnerships and empower communities to help to make healthcare more accessible for all. There’s no limit to what we can achieve for patients when we challenge ideas and champion individuals. Our work feels most...

**Summary**: About the role At Novartis, we don't just create life-changing medicines. We build partnerships and empower communities to help to make healthcare more accessible for all. There’s no limit to what we can achieve for patients when we challenge ideas and champion individuals. Our work feels most rewarding when we stretch ourselves with the full...

**Summary**: About the role The Associate Technical Project Leader will, jointly with the CMC team, lead and manage all technical development activities for assigned projects ranging from small molecules to large molecules within Technical Research & Development (TRD); represent TRD as core member in global project teams to define the global CMC strategy for...

Summary:About the role At Novartis, we don't just create life-changing medicines. We build partnerships and empower communities to help to make healthcare more accessible for all. There's no limit to what we can achieve for patients when we challenge ideas and champion individuals. Our work feels most rewarding when we stretch ourselves with the full support...

394730BR **Senior Expert - Device Project Analyst (f/m/d)**: Austria **About the role** **Location: Schaftenau, Austria, Hybrid Working #LI-Hybrid** **About the Role**: **Key Responsibilities**: Your responsibilities include, but are not limited to: - As member of global CMC analytical sub team and device sub team for your project(s) you are contact...

Summary:About the role The Associate Technical Project Leader will, jointly with the CMC team, lead and manage all technical development activities for assigned projects ranging from small molecules to large molecules within Technical Research & Development (TRD); represent TRD as core member in global project teams to define the global CMC strategy for the...

We are looking for an Analytical Project Leader to join a global team of highly skilled analytical project managers with presence in all biologics technical research and development sites of Novartis in Europe. We are looking for you as an experienced, curious, inspiring Analytical Project Leader to join our teams in Austria to support development of...