Risk Manager

**Summary**: Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities - all to bring our medicines to patients...

**QA Manager (d/f/m), Schaftenau, Tyrol, Austria** 25! This is the number of Novartis production sites that our Austrian External Supplier Organization (ESO) Team supports all over the globe. Being part of the ESO team you will be working in a very international team with a lot of global interaction and attractive tasks. As a QA Manager, you will ensure...

**Summary**: Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities - all to bring our medicines to patients...

**Summary**: The Position: As Project Manager with Novartis Austria, you will be responsible for planning and executing CAPEX projects within organization including all reporting requirements. You will be expected to deliver these projects on time, within budget and to the expected high quality. Furthermore, you will adhere to the highest safety standards...

**Summary**: As a Senior Project Manager within Novartis Austria, you will be responsible for planning and executing projects with a particular focus on pharmaceutical transfers with CAPEX investment. You will ensure timelines of each sub workstreams (Transfer, Procurement, Technical, Quality and Supply) are met and the project remains within budget. You...

**Manager Regulatory Affairs (f/m/d), Schaftenau/Kundl, Tyrol, Austria** 8! This is the number of high-quality biosimilars for which Sandoz has already received a marketing authorization, and that provided increased access to life-saving medicines to patients worldwide. Additionally, Sandoz has a rich pipeline of further biosimilars under development.**Your...

395087BR **External Communication Manager (f/m/d)**: Austria **About the role** **External Communication Manager (f/m/d)** **Location: Tyrol/Vienna, Austria** Internal role title: External Engagement Senior Manager (M/F/d) In this role you’ll deliver the external Communications and Engagement (C&E) strategy for Novartis in Austria and our key therapy...

**(Senior) Regulatory Manager (f/m/d), Kundl/Schaftenau, Tyrol, Austria** 576! That is the total number of projects and products on our Global Regulatory Affairs CMC (Chemistry, Manufacturing, Control) project list. All of these innovative projects are aimed at making a difference in patients’ lives, and we need your help. As a member of our Global...

**Summary**: The Position: As Project Manager with Novartis Austria, you will be responsible for planning and executing CAPEX projects within organization including all reporting requirements. You will be expected to deliver these projects on time, within budget and to the expected high quality. Furthermore, you will adhere to the highest safety standards...

**About the Role**: **External Communication Manager (f/m/d)** **Location: Tyrol/Vienna, Austria** Internal role title: External Engagement Senior Manager (M/F/d) In this role you’ll deliver the external Communications and Engagement (C&E) strategy for Novartis in Austria and our key therapy areas. You will be developing communications strategy and...

**Summary**: The External Operation Manager (EOM) is accountable for the seamless execution of the sourcing and supply strategy for comparators and other open label non-Novartis commercial drugs used in clinical trials across the Global Clinical Supply (GCS). They serve as primary interface between the external partner (CMO), internal functions and extended...

**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**: - 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**: Verantwortlich für regulatorische Aktivitäten insbesondere in den Bereichen Chemie, Herstellung und Kontrolle (CMC). Aktivitäten wie die Vorbereitung und Veröffentlichung von REG CMC-Dokumentation für Einreichungen bei Gesundheitsbehörden. Interagieren Sie außerdem mit HA's auf REG CMC-Fragen, um neue Produkte oder Markteinführungen zu...

**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**: Location: Schaftenau, Austria Role Purpose: Provide quality assurance expertise, guidance and support to operational activities in development and research organizations to ensure compliance with applicable regulatory requirements and Novartis procedures and quality standards. Manage projects, including Quality Plan initiatives, and processes...

**Summary**: **About the Role**: **Key Responsibilities**: - Leads or contributes to selected cross-functional and high priority projects in alignment to GCS strategy, from start to completion. - Responsible to deliver assigned projects on time, within scope, within budget and with quality (e.g. timely execution of cross-functional plans, accurate...

300 million! This is the number of people worldwide who are suffering from autoimmune disease and who would benefit from less expensive medication. As a Human Factors Engineering Expert (M/F/d), you will be responsible to design drug delivery systems to meet the needs of our patients in collaboration with other teams and partners, to enable new combination...

**Summary**: **About the Role**: **Key Responsibilities**: - Represent GCS/Technical Research & Development (TRD) in the Global Clinical Trial Team (GCT) and act as business partner to support and influence the decision-making process on the supply strategy and packaging design to be adopted in clinical trials. Attends TRD sub-team meeting providing...