CSL's R&D organization is accelerating innovation to deliver greater impact for patients with a project-led structure and a focus on collaboration
Job Summary
CSL's R&D organization is accelerating innovation to deliver greater impact for patients with a project-led structure and a focus on collaboration.
You will be responsible for preparing adequate Pharmacovigilance assessments in the course of GMP deviation investigations, complaint investigations and other reports on a high scientific level and in close cooperation with relevant stakeholders.
CSL Behring is a global biotherapeutics leader driven by our promise to save lives, focused on serving patients’ needs by using the latest technologies.
Matching Summary
CSL's R&D organization is accelerating innovation to deliver greater impact for patients with a project-led structure and a focus on collaboration.
Skills & Requirements
Must-have
Pharmacovigilance assessments
GMP deviation investigations
Complaint investigations
Regulatory framework knowledge
International regulations and standards
Nice-to-have
Agile team commitment
Dynamic biotech ecosystems
High scientific level communication
Cultivated interpersonal level communication
Self-responsible and flexible
Key Requirements
University graduate (Diploma/MA/MS, PhD) in life-sciences
Technical knowledge of PV and quality regulatory framework
Good knowledge of international regulations and standards (GVP, GMP)