Manager, Regional Regulatory Strategy

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 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: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...

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...

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...

The Life Science Career NetworkOur client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a world-leading...

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...

Salary:Highly CompetitiveJob type:PermanentDiscipline:Project ManagerLocation:Switzerland- Basel, Schweiz Posting date: 27 Feb 2024Reference:57992Proclinical are recruiting for a Regulatory Affairs Manager - EMEA to join a pharmaceutical organisation. This role is on a permanent basis and is located within the EMEA with the ability to either work remotely or...

Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.Manager, Regulatory Affairs,...

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,...

EINFÜHRUNG:Our profession and our passion are "HR Management".Global Personal is an independent company of the Interiman Group SA with over 100 employees offering a complete range of services in the field of Human Resources at 21 locations in German-speaking Switzerland.For our client, an international technology company in Basel, we are looking for...

For our customer located in Basel/Switzerland we are currently looking for a:Regulatory Affairs CMC Associate Manager (M/F/x)**- pay rate range - given by our client: 51 chf/h*Hiring Manager Job Description: As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high quality CMC regulatory documentation for our...

For our client, an international pharmaceutical company in Zurich, we are in search for a Senior Regulatory CMC Manager (f/m/d).Responsibilities: Prepare CMC responses to health authority questions during development, registration and product lifecycle Identify the required documentation for global submissions and negotiate the delivery of approved technical...

For our client, a leading pharma company in Basel, we are looking for a Regulatory Affairs CMC Associate Manager to start asap.Contract duration: 18 months with extension possibleWorkload:100%Location: Basel cityDescription:As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high-quality CMC (Chemistry,...

For our customer located in Basel/Switzerland we are currently looking for a: Regulatory Affairs CMC Manager (M/F/x)Tasks & Responsibilities / Must Haves Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation & publication of REG CMC documentation for submissions to Health...

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...

Posted: Today Location: Basel, Switzerland Job Ref: BH Job Type: Contract Salary:CHF40 CHF44 per hourExpiry date: 1/18/2023 Contact:Audwin CheungXplore Life Sciences are recruiting for an Associate Regulatory Affairs CMC Manager to work for a Global Leader in Pharmaceuticals based in Basel.This is an 18 Month freelance contract and you must have valid right...

Die Gesundheit und die Lebensqualität von Patienten zu verbessern, ist das Ziel des forschenden Pharmaunternehmens Boehringer Ingelheim. Seit der Gründung im Jahre 1885 in Familienbesitz, zählt Boehringer Ingelheim zu den 20 führenden Unternehmen der Branche. Für die drei Geschäftsbereiche Humanpharmazeutika, Tiergesundheit und Biopharmazeutika...