Arrowhead Pharmaceuticals · 10 hours ago
Specialist II, Supplier Quality
Verona, WI
Full-time
Onsite
Mid Level
$70K/yr - $85K/yr
3+ years expArrowhead Pharmaceuticals, Inc. is a clinical stage biopharmaceutical company focused on developing innovative drugs that treat intractable diseases. The Specialist II, Supplier Quality role is responsible for providing quality assurance support for the Supplier Quality Management program, ensuring compliance with quality standards and managing supplier-related quality events.
BiotechnologyHealth CareNanotechnologyPharmaceutical
No H1B
Responsibilities
Support supplier qualification, requalification, and ongoing monitoring activities for raw material suppliers, CMOs, contract laboratories, packaging vendors, and service providers
Assist with supplier risk assessments and ensure documentation is current and compliant
Collaborate with stakeholders and suppliers, as needed, on quality events and non-conformances and issue supplier corrective action requests, as outlined in the applicable quality agreements
Assist with maintenance of approved supplier lists and supplier quality records
Review and assess supplier change notifications for quality and regulatory impact
Ensure timely and accurate documentation within the Quality Management System (QMS)
Track and trend supplier performance metrics (e.g., deviations, on-time CAPA closure, audit findings)
Identify recurring issues and support continuous improvement initiatives
Assist with preparation, update, review, and routing of Arrowhead procedural documents
Assist with other QA duties as needed
Qualification
Required
BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry is preferred
3 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization with an emphasis on Supplier Quality
Working knowledge of 21 CFR Parts 210/211, ICH Q7, and applicable global regulatory expectations (e.g., FDA, EMA, Health Canada), along with familiarity with relevant regulatory guidance documents
Preferred
Prior experience with use of an electronic document management system in a regulated environment
Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and Smartsheet
Excellent interpersonal, verbal, and written communication skills
Ability to consistently communicate with external parties in a professional manner
Ability to follow company procedures, work instructions, and policies
Excellent attention to detail and organizational skills
Ability to work independently with minimal supervision as well as manage priorities within a face-paced environment
Benefits
Competitive salaries
Excellent benefit package
Company
Arrowhead Pharmaceuticals
Arrowhead Pharmaceuticals is a biotechnology company that focuses on the development of medicine to treat diseases with a genetic origin.
501-1000 employees
Funding
Current Stage
Public CompanyTotal Funding
$2.45BKey Investors
Sarepta TherapeuticsSixth StreetSilence Therapeutics
2026-01-07Post Ipo Equity· $200M
2026-01-07Post Ipo Debt· $625M
2024-11-26Post Ipo Equity· $325M
Leadership Team
Christopher Anzalone
President and Chief Executive Officer
Recent News
2026-01-14
Company data provided by crunchbase