Arrowhead Pharmaceuticals

HQ
Pasadena
Total Offices: 4
352 Total Employees
Year Founded: 2004

Arrowhead Pharmaceuticals Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers occupational accident insurance

Offers disability insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Offers company equity

Offers employee discounts

Offers performance bonuses

Offers dental insurance

Offers health insurance

Offers Health Savings Account (HSA)

Offers Flexible Spending Account (FSA)

Offers vision insurance

Work-Life Balance + Wellbeing

Offers generous PTO

Provides paid holidays

Provides bereavement leave

Offers paid volunteer time

Provides paid sick days

Provides military leave

Company Culture

Provides free snacks and drinks

6 Days AgoSaved
In-Office
Verona, WI, USA
Pharmaceutical
Leads a team of CMC analytical scientists supporting pharmaceutical drug substance and drug product development. Oversees analytical method development, validation, characterization, GMP testing, technical documentation, regulatory CMC submissions, and vendor/CDMO collaboration. Provides scientific direction, mentoring, workload prioritization, and cross-functional project leadership while ensuring compliance with cGMP and regulatory requirements.
Pharmaceutical
Provides technical oversight and lifecycle management for externally manufactured drug substance programs. Reviews GMP batch documentation, trends process and quality data, leads deviation and root-cause investigations, supports process improvements, coordinates oligonucleotide manufacturing, and assists with technology transfer to contract manufacturers. The role also executes scale-up conjugations and bench-scale reactions while collaborating cross-functionally with process development, analytical, regulatory, quality, and manufacturing teams.
14 Days AgoSaved
In-Office
Verona, WI, USA
Pharmaceutical
Drafts, edits, and standardizes GMP documentation for deviations, investigations, CAPAs, and change controls. Translates SME input into clear, compliant, inspection-ready QMS records aligned with data integrity, cGMP, and site procedures. Coordinates with cross-functional teams to improve approval quality, supports audits and inspections, and ensures investigations include appropriate evidence, root cause analysis, corrective actions, and effectiveness checks.