Head Regulatory Affairs City, Kreis 1, Zürich Jobs

 ...worked to support the passage of numerous bills that have benefitted close to 500 million people in developing countries. Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy. This is a part-time 12-hours per... 

About the Role Key Responsibilities  Leads and develops state-of-the-art operational transfer pricing processes by driving automation and supporting initiatives for process improvements and co-ordinates the implementation of changes along the Novartis value chain and...

 ...Entreprise : For our client, a successful and dynamic store chain rapidly expanding in Europe, we are currently looking for a Head of HR to support the development and growth of the business in Switzerland. Description du poste : As part of the country... 

 ...role will require considerable cross-functional interaction, notably including QA, Regulatory Affairs, Clinical and Commercial functions. The Device Engineer will report to the Section Head of Device Engineering and will be integrated into the Roche Device Development... 

 ...Bachelor degree preferred in a technical field and/or engineering. Proven process understanding in Sterile Manufacturing (Pharma, regulatory aspects). Familiarity with GMP requirements, quality procedures and SOP execution. Previous exposure to any of the... 

 ...activities in fresh markets, documenting them comprehensively Monitor and analyse forthcoming and recently enacted tax laws, regulatory positions, legal rulings, and court cases impacting the company's direct tax position. Propose strategic action steps as required... 

 ...Create, implement, maintain, and work with Vendors on establishing Quality Agreements where needed. Interface between quality/regulatory/compliance personnel and operations to identify applicable regulatory and compliance requirements and ensure accurate understanding... 

 ...development, validation, stability, and release testing). You provide valuable input to the analytical CMC documents and support regulatory submissions. • Manage interactions and contribute to a high level of collaboration with internal and external stakeholders. •... 

 ...Experience with refrigeration and ventilation systems to ensure clean room conditions in pharmaceutical production and the associated regulatory requirements (GMP). ~ Very good communication and interaction skills with various interfaces within the company organization.... 

 ...development via the Proof of Concept mechanism, and driving the program after Proof of Concept by delivering key Profiling data to support regulatory submissions • As a recognized expert in your field, you drive project team clinical strategies and bring global credibility...