Regulatory Affairs Cmc Associate Director
vor 2 Wochen
**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 content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
- Represent Global Regulatory CMC on cross-functional project teams and maintain collaborative partnerships with stakeholders
- Initiate and lead Health Authority interactions and negotiations: setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans. Establish and maintain a single point of contact with FDA.
- Provide strategic advice and direction within the department and cross-functionally through specialized assignments.
**Minimum Requirements**:
Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biol-ogy, Biotechnology, Biology) or equivalent; advanced degree desired
- Minimum 8 years regulatory experience preferred and/or pharmaceutical industry experience
- Substantial knowledge/experience in regulatory submission and approval processes and ability to deal with complex CMC regulatory issues and requirements
- Proven ability to critically evaluate data from a broad range of scientific disciplines.
**Commitment to Diversity & Inclusion**:
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
**Join our Novartis Network**:
Division
Development
Business Unit
Pharmaceuticals
Location
Austria
Site
Schaftenau
Company / Legal Entity
AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
-
Regulatory Affairs Cmc Manager
vor 2 Wochen
Langkampfen, T, Österreich Novartis Vollzeit**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...
-
Regulatory Affairs Cmc Senior Manager
vor 2 Wochen
Langkampfen, T, Österreich Novartis Vollzeit**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...
-
Ra Cmc Postgraduate Intern
Vor 3 Tagen
Langkampfen, T, Österreich Novartis Vollzeit**Summary**: The Regulatory Affairs CMC Postgraduate Training Program in Schaftenau, Austria is an opportunity to discover the global function of Regulatory Chemistry, Manufacturing and Controls. **About the Role**: Are you interested to learn more about Regulatory Affairs Chemistry, Manufacturing and Controls (RA CMC) and the pharmaceutical...
-
Ra Cmc Submission Coordinator
vor 1 Woche
Langkampfen, T, Österreich Novartis Vollzeit**RA CMC Submission Coordinator (f/m/d), Schaftenau, Tyrol, Austria** 582! 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, your role would...
-
Ra Cmc Submission Coordinator
Vor 7 Tagen
Langkampfen, T, Österreich Novartis Vollzeit**RA CMC Submission Coordinator - Biosimilars (M/F/d), Global Drug Development, Schaftenau, Austria** **582!** 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 pa-tients’ lives and we need your support. As a member of our Global...
-
Langkampfen, T, Österreich Novartis VollzeitWe are looking for an Associate Director of Analytical Development Program Management 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...
-
Drug Product Project Leader
vor 1 Woche
Langkampfen, Österreich Novartis Pharma GmbH VollzeitDrug Product Project Leader (m/f/d) - Associate Director Science & Technology Flexible Arbeitszeiten Home Office Teilzeit möglich Überblick Novartis sucht eine Person als Projektleiter:in für Arzneimittel. Du arbeitest in der Entwicklung von biologischen Produkten. Du brauchst Erfahrung in der Arzneimittelentwicklung und Führung. Wichtig sind...
-
Regulatory Affairs Medical Device Manager
vor 2 Wochen
Langkampfen, T, Österreich Novartis Vollzeit**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...
-
Associate Director
vor 1 Woche
Langkampfen, T, Österreich Novartis Vollzeit € 78.383 - € 120.000 pro JahrSummaryLI-HybridInternal job title: Associate Director - Science & TechnologyLocation: Schaftenau, AustriaAbout the RoleKey Responsibilities: As a member of global CMC analytical subteam and device subteam for your project(s), you are the contact person & coordinator for all project-specific analytical tasks related to functional attributes of drug-device...
-
Senior QA Operations Expert
vor 19 Stunden
Langkampfen, T, Österreich Novartis Vollzeit**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...