The Process Development Lead is a key leadership role within Technical Operations, responsible for leading global process development teams and driving the development, optimization, and implementation of robust and scalable manufacturing processes for plasma-derived biotherapeutics. This
We are looking for a DP Lead parenteral Iron, to join our team in Zurich or St. Gallen, Switzerland. As part of the Integrated Product Team Iron & Small Molecules within Technical Operations, you will be
The Senior Laboratory Specialist, Tech Ops researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet clinical safety standards. Conducts
Senior CI Specialist – Value Stream Bulk Position Purpose Are you passionate about driving operational excellence and transforming performance through Continuous Improvement? As Senior CI Specialist, you will play a key role in shaping the future
We are currently looking for a Senior Scientist, Mechanistic Pharmacology in Translational Research (complex in vitro models cardiovascular and renal indications) to join our team in Schlieren, ZH. Key Tasks Develop, optimize, and apply advanced cellular
Wir suchen eine(n) motivierte(n) Associate Scientist / Senior Laboratory Specialist welche(r) unser Pilot Plant Bern Team verstärkt. In dieser Rolle übernimmst du eine zentrale Funktion bei der Hochskalierung von Entwicklungsprozessen, die künftig in unseren Produktionsanlagen implementiert
Key Responsibilities Lead end-to-end technical projects across technology transfers, product lifecycle management, and continuous improvement initiatives for assigned products and external manufacturing partners. Develop and execute robust Project Execution Plans by translating technical implementation strategies into
This role is a position in the Drug Delivery Systems & Packaging (DDSP) department within CSL Technical Operations. The ideal candidate has a solid track record in the development of drug delivery devices, from concept development through
We are currently looking for a Senior Scientist, Mechanistic Pharmacology in Translational Research (complex in vitro models cardiovascular and renal indications) to join our team in Schlieren, ZH. Key Tasks Develop, optimize, and apply advanced cellular
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: Develops
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 cycle
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output including, but not limited to: ADaM datasets, tables, figures and listings
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part
Wer wir sind CSL Behring ist ein weltweit führendes Biotherapeutika-Unternehmen, das sich der Entwicklung und Bereitstellung lebensrettender Therapien widmet. Mit unseren innovativen Produkten leisten wir einen entscheidenden Beitrag zur Behandlung schwerer und seltener Erkrankungen und verbessern die
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
About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with
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
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 data
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part
We are looking for a DP Lead parenteral Iron, to join our team in Zurich or St. Gallen, Switzerland. As part of the Integrated Product Team Iron & Small Molecules within Technical Operations, you will be