Amgen Australia is seeking an Associate Vice President of Quality to lead global quality strategies for their Research and Development Organization, focusing on various therapeutic areas. The ideal candidate will have extensive experience in clinical quality assurance and a proven track record in managing teams and overseeing large clinical programs
Job Summary
This role leads proactive end-to-end quality strategies globally for therapeutic areas including Oncology, Inflammation, Cardiovascular, and Neuroscience.
The successful candidate will drive the transformation of clinical quality oversight in compliance with ICH E6R3 and enable embedded quality oversight into clinical development teams.
Amgen offers a competitive salary range of $266,028 to $359,920 along with comprehensive benefits including retirement plans, stock incentives, and flexible work models.
Matching Summary
Match Score: 85
Amgen Australia is seeking an Associate Vice President of Quality to lead global quality strategies for their Research and Development Organization, focusing on various therapeutic areas. The ideal candidate will have extensive experience in clinical quality assurance and a proven track record in managing teams and overseeing large clinical programs.
Salary
Base: $266,028 - $359,920 USD; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible work models
Skills & Requirements
Must-have
Doctorate degree required
7+ years Clinical Quality experience
10+ years Master's degree Clinical Quality
7 years managerial experience leading teams
Risk-based quality oversight programs
ICH E6R3 compliance expertise
Health authority inspection strategy
Nice-to-have
Experience with Biosimilars and Rare Disease
Knowledge of Precision Medicine
Digital technology integration skills
Data analytics capability
Collaborative leadership style
Adaptability to changing environments
Key Requirements
Doctorate degree with 7 years experience OR Master's with 10 years OR Bachelor's with 12 years
7 years of direct people management experience
Proven track record managing health authority inspections
Working knowledge of global regulatory environment for drug development