Job Opportunities

The Principle Scientist, CMC Science is responsible for supporting and executing Chemistry, Manufacturing, and Controls (CMC) strategies for pharmaceutical and/or biologic products across clinical dev

The Scientist, Tech Ops researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monito

Senior Scientist (Pathogen Safety) Position Description Summary​ The Senior Scientist, Tech Ops contributes to routine technical tasks and supports project teams by performing specific functions su

Position Description Summary: The Principal Scientist PK/QSP will lead and manage nonclinical PK/QSP strategies across multiple drug development projects. This role serves as the primary PK/QSP repr

Position Description Summary: The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support model

This role supports the discovery, development, and progression of new medicines for unmet medical needs from early research to clinical development and commercialization. Responsibilities include exec

im Else Kröner Fresenius Zentrum für Digitale Gesundheit im Bereich Gastroenterologie und Endoskopie Die Stelle ist zum in Voll- oder Teilzeitbeschäftigung für zunächst 18 Monate befristet zu beset

HUMAN bietet sichere Labordiagnostik in mehr als 160 Ländern. Wie wir das schaffen? Mit zuverlässigen Reagenzien und Analysesystemen sowie mit Mitarbeitern, die Kundenorientierung leben und zur Verbes

For a large European automotive manufacturer, we are building powerful Business Analytics solutions on top of a data warehouse. To grow this team, we are looking for an experienced Software Developer

???? Device Engineer / Scientist (m/w/d) – Design Verification & Medical Devices (MDR/FDA) HIER WERDEN SIE ARBEITEN: Sie sind auf der Suche nach einer neuen beruflichen Herausforderung?Dann sind Sie b

???? Device Engineer / Scientist (m/w/d) – Design Verification & Medical Devices (MDR/FDA)HIER WERDEN SIE ARBEITEN:Sie sind auf der Suche nach einer neuen beruflichen Herausforderung?Dann sind Sie bei

???? Device Engineer / Scientist (m/w/d) – Design Verification & Medical Devices (MDR/FDA) HIER WERDEN SIE ARBEITEN: Sie sind auf der Suche nach einer neuen beruflichen Herausforderung?Dann sind Sie b

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world e

Position Purpose The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is

For our CSL Behring Operations / Manufacturing, we are looking for a Head of Manufacturing Engineering and Maintenance Closing Date for Applications – 17th April 2026 The Head of Manufacturing Eng

We are looking for a strategic and collaborative Regional Regulatory Lead (RRL) to join our Global Regulatory Affairs team. In this role, you will lead both strategic and operational regulatory activi

The Analytical Strategy Director is a senior scientific and strategic leadership role responsible for designing and overseeing analytical strategies that support drug discovery, development, and regul

Position PurposeThe Head of Global Regulatory Affairs CMC - Network Strategy & Operation is responsible for:Partnering closely with global and regional Global Regulatory Affairs colleagues, as well as

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 goa

Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Ther

CSL's 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

Role Summary The Senior Biostatistician provides, and may lead, statistical contributions to a clinical development program. The Principal Biostatistician implements statistical strategies for clinic

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regul

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

Overview: The Manager, Clinical Trial Authorization (CTA) is responsible for ensuring that CTA activities for assigned clinical studies are planned, governed, and overseen in line with CSL regulatory