Senior Manager, GxP Systems & Validation

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein.

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics.

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI.  Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

The Senior Manager GxP Systems & Validation provides strategic and operational leadership for GxP-regulated computerized systems across their full lifecycle. This role is accountable for governance, validation strategy, inspection readiness, and compliant system administration, ensuring alignment with global regulatory requirements (FDA, EMA, MHRA, ICH) and evolving industry standards (GAMP 5, CSA).

This leader serves as a key partner to Manufacturing, Quality, CMC, CSA and Compliance, GLP Operations, and external vendors, driving scalable compliance frameworks while enabling business agility. The role combines system ownership and administration, validation project management, and organizational oversight to ensure enterprise-wide data integrity and computerized system compliance.

Responsibilities

Strategic Leadership & Governance

* Maintain governance frameworks for GxP computerized systems

* Define validation strategies aligned with GAMP 5 and CSA principles

* Support modernization initiatives (e.g., SaaS adoption, cloud validation, CSA transition)

* Serve as system owner and system administrator for critical GxP platforms

* Maintain validation and system lifecycle policies and standards

* Participates in continuous improvement of validation methodologies, templates, and risk-based approaches

* Provide compliance guidance to executive leadership and functional heads

System Lifecycle Oversight

* Oversee administration and compliant operation of GxP systems (Laboratory systems, LIMS, MES, EDMS, enterprise SaaS platforms)

* Ensure systems remain validated, secure, and audit-ready throughout implementation, upgrades, and decommissioning

* Approve system configurations, changes, and access governance frameworks

* Ensure robust data integrity controls in accordance with ALCOA+ principles

* Monitor system performance, audit trails, cybersecurity controls, and vendor compliance

Validation Program Leadership

* Lead enterprise validation initiatives across multiple concurrent projects

* Oversee development and approval of validation deliverables (URS, Risk Assessments, IQ/OQ/PQ, Traceability, Summary Reports)

* Ensure appropriate application of risk-based validation and CSA methodologies

* Manage validation master planning and resource allocation

* Provide oversight of regression testing and revalidation strategies

* Ensure validation documentation supports global inspection readiness

* Act as SME during regulatory inspections and internal audits

* Oversee remediation efforts related to audit findings, deviations, and CAPAs

* Maintain awareness of…