Vp, Legal Regulatory Strategy

The Role:The Director, Regional Regulatory Strategist - ID will have the opportunity to lead the regulatory strategy with the European Medicines Agency (EMA), act as the regulatory strategy partner for International countries, and provide regulatory support to the VP, Regulatory Affairs International. This is a new role intended for a forwardlooking,...

The Role:The Manager of Regulatory Strategy-International based in Basel, Switzerland will have the opportunity to provide regulatory support to the Senior Director, Regulatory Affairs Strategy, Infectious Disease. This is a newly created role intended for a forward looking, creative and agile regulatory manager able to anticipate and address the challenges...

The Role:The Manager of Regulatory Strategy-International based in Basel, Switzerland will have the opportunity to provide regulatory support to the Senior Director, Regulatory Affairs Strategy, Infectious Disease. This is a newly created role intended for a forward looking, creative and agile regulatory manager able to anticipate and address the challenges...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide,...

Global Regulatory Affairs DirectorWe are looking for a person who will develop/lead/implement regulatory strategy through a global regulatory team approach for assigned projects or product(s) across all phases of product development, and ensure timely development of regulatory strategy and operating plans.Responsibilities Participate in or lead departmental...

The Role:Here's What You'll Do:Provide leadership for regulatory CMC aspects of product development projectsLead and drive all CMC submission activities (planning,Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelinesDevelop effective CMC regulatory strategies for submissions (e.g. IND/CTA/BLA/MAA)...

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide,...

The Role:Here's What You'll Do:Develop and contribute to content, format and accountability for regulatory submissions and related supplements and amendments, including EMA regulatory documents such as meeting requests, briefing books, orphan drug designations, DSURs, MAA etc.)Work with the International local regulatory leads in Canada, Asia, Latin America...

VectivBio is a global, clinical-stage biotechnology company focused on the discovery, development, and commercialization of innovative treatments for severe rare conditions with high unmet medical need. VectivBio is now a part of Ironwood Pharmaceuticals, Inc., a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of...

Job ID REQ May 07, 2024 Switzerland SummaryThe Global Program Regulatory Director (GPRD) Medical Device & IVD Excellence EU & ROW provides global regulatory leadership throughout the lifecycle of a development and/or marketed product program(s). Using prior education and experience, the GPRD Medical Device & IVD Excellence EU & ROW integrates multiple...

Job ID REQ May 07, 2024 Switzerland SummaryThe Global Program Regulatory Director (GPRD) Medical Device & IVD Excellence EU & ROW provides global regulatory leadership throughout the lifecycle of a development and/or marketed product program(s). Using prior education and experience, the GPRD Medical Device & IVD Excellence EU & ROW integrates multiple...

THE POSITION:This role of is the senior most regulatory role within EPD in the Emerging Market business unit_. _As a leader, the role of the Director, Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to support and partner the business by ensuring the successful development, manufacture and distribution of products in...

Switzerland, Basel Switzerland, VispToday, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers....

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.Abbott...

500 The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority...

394918BRGlobal Program Regulatory Manager (GPRM - Cardiometabolic):SwitzerlandAbout the role26 major approvals, 13 major submissions and 2,000 associates worldwide. That was Regulatory Affairs in 2020. We are a culturally diverse, global team of talented professionals seeking to leverage the voices of our patients in our approach to bringing potentially...

Contract Type: PermanentClosing date:Reference: VN1710 Who we are Vectura Fertin Pharma's ambition is to become a marketleading wellness and healthcare business.Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems. We are...

386786BRLegal Trainee Innovative Medicines & Development:SwitzerlandAbout the roleNovartis provides healthcare solutions that address the evolving needs of patients and societies worldwide. Our broad portfolio includes innovative pharmaceuticals and oncology medicines. Our mission is to discover new ways to improve and extend people's lives. Our vision is to...

We are currently looking for an agile and technically excellent senior-level lawyer to join and lead our Legal Sourcing & Intellectual Property (IP) EMEA team.Your field of responsibilityYou will manage a team of lawyers based in Zurich and Wroclaw, working together to provide legal support on third-party supplier sourcing contracts (such as software,...

Job PurposeBe a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Canada, perform product registration in EU, US & Canada. Main Tasks and ResponsibilitiesSupport product development process and ensure compliance of deliverablesCompile the Regulatory...