Fachspezialistin Regulatory Compliance

The Role:Reporting to the Director Quality Systems & Compliance the AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna's product with the registered dossiers.Here's What...

The Role:The Sr. Director of Regulatory Process and Compliance position will work cross-functionally to drive activities that will ensure a state of continuous compliance at Moderna and build inspection-preparedness capabilities and sustain a positive compliance reputation between Moderna's business partners, Health Authorities and cross-functionally within...

**Lege bei KPMG den Grundstein für deine berufliche Laufbahn und bringe dein Wissen vom Studium aktiv ein. Wir sind ein dynamisches Team, das Finanzdienstleister zu regulatorischen, finanzmarktrechtlichen und Compliance relevanten Themen berät.**Graduate - Regulatory & Compliance Financial ServicesSo bringst du KPMG weiter- Berate zusammen mit den...

**Freelancer - Banking Regulatory & Compliance**:- Unterstütze uns mit deinem Know-how in KYC, AML und Compliance und erhalte die Möglichkeit dein einzigartiges Netzwerk weiter auszubauen.- Zürich- nach Vereinbarung- 100 %, 4-6 Monate**So bringst du KPMG weiter****:- Unterstütze bei KYC, AML und Background Checks- Du gibst Support bei Projekten und...

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...

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...

Reference Code: 93955Trade Compliance Intern: Richemont VillarssurGlâne, FR, CH Trainee/InternRichemont owns some of the world's leading luxury goods Maisons, with particular strengths in jewellery, fine watches and premium accessories. Each Maison represents a proud tradition of style, quality and craftsmanship and Richemont seeks to preserve the heritage...

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 PurposeAs Team Leader Regulatory & Compliance - Regenerative Solutions, you will be part of a small but highly motivated and very international team, dedicated to our regenerative product portfolio. With your regulatory and compliance knowledge, you will support product developments and life cycle activities for the regenerative portfolio in order to...

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and...

General Description:The Director Regulatory Affairs will be responsible for developing and implementing regulatory strategies for the designated program to secure and maintain marketing authorization in line with business objectives, and in coordination with key internal stakeholders.Essential Functions of the job: Act as the representative of European...

General Description:Under the direction of the General Manager Sub Region Europe, this individual is responsible for the local representation of regulatory affairs and quality assurance in SRE. The incumbent provides dynamic leadership, strategic direction and close oversight of all regulatory affairs and compliance activities in SRE across BeiGene's...

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...

Stratpharma, a fast-growing Dermatology company, is currently looking for a Global Regulatory Affairs Associate to join their dynamic team. This is an exciting opportunity to be part of a company that is experiencing rapid growth and expanding globally.This is a highly successful company who have an impressive 200% year on year growth and are going through...

Would you like to specifically demonstrate your expertise in the field of pharmaceutical services in a new professional challenge in order to fully exploit your potential? Then take the next step with us As a specialised personnel service provider, the bruederlinpartner group brings specialists and managers in the field of pharmaceuticals, research and...

Your mission:We are committed to transforming healthcare and clinical research by harnessing the power of Digital Biomarker technology. Specializing in the development of innovative software as medical devices, we strive to revolutionize patient outcomes and elevate the standard of healthcare delivery.As our RAQA (Regulatory Affairs and Quality Assurance)...

About UsSygnum is the world's first regulated Digital Asset Bank, founded on Swiss and Singapore dual heritage, headquartered in Switzerland and operating globally. We make digital assets bankable, secure and convenient, empowering our clients to invest in the digital asset economy with complete trust. Sygnum's diverse and talented team of banking,...

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...

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...