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 and San Diego, CA. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

Join our Quality Assurance team as an intern and gain valuable experience in data management, documentation, and regulatory compliance. You will assist in organizing and maintaining records, improving system integration, and ensuring accurate documentation to support business operations. This role provides an opportunity to collaborate with cross-functional teams, enhance workflows, and contribute to regulatory readiness. Ideal for students looking to develop skills in quality management, compliance, and operational efficiency.

This is a 12-week, fully onsite Summer Internship Program paying $22.00/hr.

Responsibilities

Assist in updating and maintaining vendor records in the Quality Management System (QMS) to improve system integration and data accuracy.
Upload and organize vendor licenses, certificates, and agreements, ensuring proper tracking and accessibility.
Support document management and compliance efforts, including linking records across systems for streamlined access.
Assist in data consistency and quality control, ensuring accurate and up-to-date information across multiple platforms.
Help prepare documentation for regulatory submissions and inspections, organizing and reviewing required materials.

Requirements:

Currently enrolled student at an Accredited University or College and majoring in Life Sciences, Quality Assurance, Regulatory Affairs, or a related field
Basic understanding of pharmaceutical quality systems (QMS) and regulatory compliance.
Excellent verbal and written communication skills
Ability to work independently while collaborating with Quality, Contracts, and Regulatory teams
Strong problem-solving skills
Eagerness to learn

California pay range

$10,560—$10,560 USD

Arrowhead provides competitive salaries and an excellent benefit package.

All applicants must have authorization to work in the US for a company.

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Arrowhead Pharmaceuticals

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