By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Position Purpose: Ensure Corporate & External Affairs liaison with commercial and site leadership in Switzerland. Provide strategic guidance and direction to the affiliate and site leadership teams on government relations, policy, and advocacy, enable early identification and
Position Summary The Senior Director, Head of Medical Evidence reports into the Vice President, Head of Disease Areas and coordinates with Medical Affairs and cross-functional stakeholders to lead the Integrated Evidence Generation Plans (IEGP) for all
Position Purpose: The Director, Senior Global Regulatory Lead (Sr. GRL) in Global Regulatory Strategy (GRS) is a member of the respective GRA GRS Therapeutic Area and contributes to the vision and goals of CSL as follows:
Role Overview: The Senior Director of Market Access for Inline Assets will be responsible for shaping and implementing market access strategies for CSL Behring inline assets. This role is accountable for maximizing the asset total life
Requirements Engineering: You support the creation, documentation, and management of traceable requirements for various subsystems in our next-generation DAC development projects. Software Transition: You assist in the migration of requirements and engineering data from one software
Requirements Engineering: You support the creation, documentation, and management of traceable requirements for various subsystems in our next-generation DAC development projects. Software Transition: You assist in the migration of requirements and engineering data from one software
Job Details Senior Technology Development Specialist (80-100%) at Climeworks, Opfikon, Zurich, Zürich, Switzerland. Responsibilities Sorbent Module Development: You take ownership of developing and maturing innovative sorbent modules from concept phase (TRL0) to early-stage product readiness (TRL5),
Job Details Senior Technology Development Specialist (80-100%) at Climeworks, Opfikon, Zurich, Zürich, Switzerland. Responsibilities Sorbent Module Development: You take ownership of developing and maturing innovative sorbent modules from concept phase (TRL0) to early-stage product readiness (TRL5),
At Sunrise, we think bigger, go further and create new ideas. For us working culture means achieving great things together. It’s where respect and innovative ideas combine with real teamwork – every voice counts, every perspective
Climeworks is a leading high‑quality carbon removal provider, combining decades of expertise in Direct Air Capture (DAC) technology with a holistic approach to carbon removal solutions. Climeworks advises companies on their carbon removal strategies and provides
Climeworks in Opfikon, Zürich is seeking an experienced professional to drive their commercial growth engine. The role includes building strategies to generate demand, orchestrating growth initiatives, and leading a high-performing team while ensuring alignment across various functions. The
About the role As the Design Governance Lead, you will establish and safeguard Takedas global design governance framework, ensuring that critical engineering and CAPEX decisions are made through a consistent, transparent, and evidence-based process. You will
Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information
Specifications and design : You lead the development of fit-for-purpose mechanical specifications, design philosophies, and basis of design for execution Globally. You ensure owner requirements are clearly defined, documented, and communicated to contractors, and validate design
The Principal, Clinical Data Management Lead provides leadership and oversight for clinical data build, programming, and vendor deliverables across in-house, hybrid, and outsourced studies, ensuring alignment with CSL standards, regulatory requirements, and industry best practices . The