Senior Manager, QMS Programs

Company: Arrowhead Pharmaceuticals
Location: Verona
Posted on: February 19, 2026

Job Description:

Job Description Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical 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 Work cross-functionally to drive and champion projects related to continuous improvement of the systems, processes, and functions comprising the GxP Quality Management System (QMS), while ensuring compliance with regulatory requirements, industry standards, and company policies in support of the development, manufacturing, testing, release, and distribution of pharmaceutical and device products (clinical and commercial). Provide expertise on the quality systems and associated processes operating across the regulated environment. Coordinate and guide audit and inspection activities, including internal audits, partner audits, and regulatory health authority inspections. Responsibilities Identify, champion, and drive cross-functional improvement initiatives to enhance and streamline quality systems, frameworks, and associated processes. Facilitate stakeholder engagement to ensure quality systems are continuously monitored and improved to strengthen compliance and operational efficiency. Plan, coordinate, and participate in internal audit activities, including preparation, execution, response coordination, and follow-up of observations. Coordinate partner audit activities, including preparing, hosting, coordinating response development, and overseeing commitments and CAPAs. Coordinate and support regulatory health authority inspection readiness efforts (e.g., GMP, GDP), including logistics planning and inspection hosting support. Develop, review, and approve a variety of controlled documents in alignment with regulatory requirements, relevant guidance, and company standards. Facilitate quality management reviews and support the development of registers, KPIs, metrics, and dashboards as well as mechanisms for routine reporting. Apply project management and execution methodologies to prioritize, plan, and deliver quality system and compliance initiatives in collaboration with stakeholders. Monitor evolving regulatory requirements and guidance, and partner with stakeholders to assess and address potential impacts to the quality system. Foster a culture of quality, collaboration, and accountability within the team and across the organization. Perform additional duties as requested. Requirements: Bachelor's degree in life sciences, pharmacy, chemistry, or related field. 8 years of experience in the regulated pharmaceutical and/or biotechnology industry, in which at least five (5) of those years were in a leadership position with increasing levels of responsibility. Full knowledge of GxP regulations, including GMP (FDA, EU, etc.), ICH guidelines, and ISO standards. Demonstrated skills in the areas of project management, organization, and execution as well as priority setting. Proven experience developing and/or improving QMS, QE, and compliance programs. Highly motivated, strategic thinker with a focus on continuous improvement and innovation, who endeavors to anticipate and resolve problems. Excellent communication, interpersonal, and leadership skills, with the ability to work with a diverse range of professionals and influence stakeholders at all levels. Previous experience with the use of electronic document / quality management systems (EMDS / EQMS). Ability for occasional business travel. Preferred: Additional Quality/Regulatory related certification desired, such as CQA, CQMP, RAC, etc. Advanced degree in life science Wisconsin pay range $145,000—$165,000 USD Arrowhead provides competitive salaries and an excellent benefit package. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Keywords: Arrowhead Pharmaceuticals, Dubuque , Senior Manager, QMS Programs, Science, Research & Development , Verona, Iowa