Public Affairs Lead - Zurich

Als Public Affairs Lead für die Schweiz treibst du die Advocacy-Strategie von Oviva in einer sich schnell entwickelnden digitalen Gesundheitslandschaft voran. · ...

We are seeking an experienced Global Regulatory Affairs Lead (m/f/d) to join our Technology (R&D) team in Lucerne. · Develop and implement global regulatory strategies for new and existing products. · Maintain a centralized regulatory database with 100% accuracy and accessibility ...

GC International AG is a global leader in dental care and oral health seeking an experienced Global Regulatory Affairs Lead to join their Technology team in Lucerne. · ...

The Regional Medical Lead – Oncology Pipeline will play a critical role in preparing the organization for successful launches of new therapeutic areas and assets while ensuring patient needs remain at the center of all initiatives. · ...

Are you passionate about shaping medical strategies building high-performing teams and ensuring readiness for new therapeutic areas and assets Do you thrive in a dynamic environment where collaboration patient focus drive success If so the role of Regional Medical Lead – Oncology ...

Are you passionate about shaping medical strategies building high-performing teams and ensuring readiness for new therapeutic areas and assets Do you thrive in a dynamic environment where collaboration and patient focus drive success If so the role of Regional Medical Lead – Onco ...

+ Oncology Medical Lead  · The Regional Medical Oncology Lead (Pipeline) will play a critical role in preparing the organization for successful launches of new therapeutic areas and assets while ensuring patient needs remain at the center of all initiatives. · +Lead the developme ...

Are you passionate about shaping medical strategies, building high-performing teams, and ensuring readiness for new therapeutic areas and assets? Do you thrive in a dynamic environment where collaboration and patient focus drive success? · ...

Blackfield Associates are supporting a renowned pharmaceutical client based in Switzerland who have a requirement for a Senior Director Regulatory Affairs CMC to join their team and lead from the front both in strategy and team directive. · Manage regulatory submissions for assig ...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. · We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our b ...

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

We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when ...

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 ...

Lead strategic, high‑impact projects across Internal Operations to align medical and marketing areas, optimise portfolio processes and deliver projects that advance Novo Nordisk's mission. · ...

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. · ...

Lead strategic projects across Internal Operations to align medical and marketing areas. · ...

We are looking for a proactive · and motivated individual with · a strong scientific background · and a genuine interest in regulatory affairs · and sustainability (R&S).This position is based in our R&S dept. · at our headquarter in Zurich. · ...

Manage regulatory activities for assigned Daiichi Sankyo products in Switzerland. · ...

At Genmab we are dedicated to building extraordinary futures together by developing antibody products and groundbreaking KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. · ...

+Job summary · Blackfield Associates are supporting a renowned pharmaceutical client based in Switzerland who have a requirement for a Senior Director Regulatory Affairs CMC to join their team lead from the front both in strategy and team directive. · +QualificationsEducated to B ...