Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them.
Requirements
- Minimum of a bachelor's degree in a science discipline, or equivalent required.
- Minimum of eight (8) years of experience working in a regulated environment with preference to quality assurance and/or manufacturing experience or equivalent required.
- Excellent written and verbal communication skills and ability to communicate effectively with internal and external parties.
- Ability to work with diverse professionals and promote cooperation, shared understanding, and commitment to ensuring best in class quality assurance protocols.
- Highly motivated team player willing to contribute to a growing pharmaceutical organization.
- Ability to work independently and manage priorities within a fast-paced environment.
- A detail-oriented self-starter who endeavors to anticipate and resolve problems and seeks opportunities to grow their role and responsibilities at Arrowhead.
- Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents.
- Understanding of document control requirements in an FDA regulated organization.
- Ability for occasional business travel.
Benefits
- Competitive salaries
- Excellent benefit package
- Generous Paid Time Off
- 401k Matching