Regulatory Affairs - Nottwil, LU

These are your tasks · Provide high quality regulatory affairs-related services for investigators in the field of patient-oriented research with a risk-based approach (e.g. review of study protocols and other essential study documents) · Promote the implementation of the ICH Good ...

These are your tasks · Provide high quality regulatory affairs-related services for investigators in the field of patient-oriented research with a risk-based approach (e.g. review of study protocols and other essential study documents) · Promote the implementation of the ICH Good ...

Provide high quality regulatory affairs-related services for investigators in the field of patient-oriented research with a risk-based approach (e.g. review of study protocols and other essential study documents). · ...

We are looking for a Regulatory Affairs Lead to join our team in Baar (Zug-Switzerland). The mission of this role is to own and drive Switzerland Local Regulatory Affairs for the MAH, ensuring end-to-end compliance across Swissmedic and FOPH/BAG requirements. ...

We are looking for a Regulatory Affairs Lead to join our team in Baar (Zug-Switzerland). The mission of this role is to own and drive Switzerland Local Regulatory Affairs for the MAH... · ...

· This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Head of Regulatory Affairs in Switzerland. · In this role, you will lead regulatory strategy and engagement across the European Union, shaping policies that enable the growth an ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications lifecycle activities. · The role focuses on EMA submissions authority interactions post-authorisation maintenance for centrally authorised medicinal products. · Lead ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities and supporting new MAAs. · Bachelor's degree in Life Sciences, Pharmacy, Engineering , or related field. · 5+ years' experience in EU Regu ...

+ As Manager, Regulatory Affairs you will lead regional RA activities for biosimilars beyond centralized authorizations coordinating with Affiliate RA to identify and fulfill national regulatory requirements to support successful product launches.+ You are a motivated and quick l ...

We are looking for a Regulatory Affairs Director – Pediatrics to develop and implement regulatory strategies for pediatric development projects. · MSc- degree in Pharmacy, Chemistry, Biochemistry, Biology or comparable · 10+ years' experience in drug development · ...

As Manager Regulatory Affairs you will lead regional RA activities for biosimilars beyond centralized authorizations coordinating with Affiliate RA to identify and fulfill national regulatory requirements to support successful product launches. · ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities, and supporting new MAAs. · ...

+ Lead regional Regulatory Affairs activities for biosimilars beyond centralized authorizations. · + Oversee product updates across multiple countries and manage key national regulatory process steps. · + Build strong relationships with affiliate and distributor teams to support ...

The Regulatory Affairs Manager is responsible for supporting and managing EU Marketing Authorisation Applications (MAA), lifecycle activities and supporting new MAAs. · ...

· At Coty, you'll get to work in a passionate team of experts, with the freedom to make an impact and have some fun along the way. · RESPONSIBILITIES · As the Manager of Regulatory Product Compliance, PIF & Registration, you are responsible for contributing to overall regulator ...

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Director, CMC Regulatory Affairs in Switzerland. · Lead CMC regulatory strategy for investigational and early commercial biological products across global teams · Advise cross-func ...

We are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. · Act as a senior regulatory expert with a focus on CMC · ...

Azurity Pharmaceuticals busca a un Global Head de Asuntos Regulatorios para liderar su equipo global. El candidato deberá tener experiencia en regulaciones farmacéuticas y capacidad para desarrollar estrategias globales. · ...