We’re seeking a proactive and experienced Supplier Quality Manager to lead our supplier oversight program and ensure... regulatory changes and ensure supplier activities meet GMP, CFR, ICH, and QAA requirements. Maintain a database of supplier...
a people manager, a program lead, or both. You will lead cross-functional collaboration within and outside AQS and decision... programming activities for multiple clinical trials within a program or an indication /disease area, or development program...
of trial and program level regulatory documents Driving execution of the assigned clinical program and/or clinical trial..., where applicable Support the Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section...
of trial and program level regulatory documents Driving execution of the assigned clinical program and/or clinical trial..., where applicable Support the Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section...
and contribute to clinical sections of trial and program level regulatory documents (e.g., investigator’s brochures, briefing books... development of clinical study report, publications and internal/external presentations Support the Global Program Clinical Head...