Specialist III, Supplier Quality

Arrowhead Pharmaceuticals•Verona, WI

3h•$85,000 - $95,000

About The Position

The purpose of this position is to provide quality assurance support for the Supplier Quality Management program in all aspects of qualification, monitoring, and continuous improvement of suppliers, contract manufacturers (CMOs), contract testing laboratories, and material suppliers. This person will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development as well as commercial programs at Arrowhead Pharmaceuticals, Inc.

Requirements

BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry
Minimum of 5 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization with an emphasis on Supplier Quality.
Prior experience working in Supplier Quality Management.
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.
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.

Responsibilities

Support supplier qualification, requalification, and ongoing monitoring activities for raw material suppliers, CMOs, contract laboratories, packaging vendors, and service providers.
Collaborate with stakeholders and suppliers, as needed, on quality events and non-conformances and issue supplier corrective action requests (SCARs), as outlined in the applicable quality agreements.
Perform quality agreement lifecycle management, including but not limited to, drafting, editing, reviewing, approving, and ensuring compliance with periodic review cycles.
Review and assess supplier change notifications for quality and regulatory impact.
Assist with supplier risk assessments and ensure documentation is current and compliant.
Ensure timely and accurate documentation within the Quality Management System (QMS).
Assist in establishing and implementing Supplier KPIs (key performance indicators) and actively contribute to the internal Quality Management Review and external Business Review meetings.
Identify recurring issues and support continuous improvement initiatives.
Assist with preparation, update, review, and routing of Arrowhead procedural documents.
Other duties consistent with the position as assigned.