PositionPrincipal Development Engineer (80–100%) at Climeworks – Opfikon, Zurich, SwitzerlandResponsibilitiesStrategic Technology Leadership: You lead the development of next-generation CO₂ collector system architectures, integrating sorbent and process requirements into scalable, manufacturable solutions.Advanced Prototyping & Validation: You drive the prototyping
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 assumptions
Technical Direction: You define and maintain the technical direction for the Electrical, Instrumentation, and Controls (EIC) Department. You lead the development of fit-for-purpose EIC specifications, design philosophies, and basis of design for execution Globally. You ensure owner
PositionPrincipal Development Engineer (80–100%) at Climeworks – Opfikon, Zurich, SwitzerlandResponsibilitiesStrategic Technology Leadership: You lead the development of next-generation CO₂ collector system architectures, integrating sorbent and process requirements into scalable, manufacturable solutions.Advanced Prototyping & Validation: You drive the prototyping
The Director Non-Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology
The Director Non-Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology
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
Responsibilities:• Manages and directs functions to comply with standard operating procedures, regulatory safety and pharmacovigilance and business technology quality standards in compliance with national and international regulations, such as relevant GxP guidelines and national and international