- Salary
- $90k - $125k
- Experience
- 3+ yrs
- Location
- Verona, Wisconsin, United States
- Job type
- Full-time
About the role
Bachelor's in a scientific/engineering discipline, 3+ years relevant industry experience with at least 3 years Regulatory CMC, experience with post-approval lifecycle management, knowledge of global health authority requirements and ICH Q12, Veeva experience, strong communication and project skills.
About Arrowhead Pharmaceuticals
Develops RNAi medicines to treat genetic and intractable diseases.
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