Senior Specialist, Quality Assurance

Arrowhead Pharmaceuticals; Verona (WI); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Competitive salaries

Excellent benefit package

Job summary

A biotech firm focused on RNA-based therapies seeks a Quality Assurance specialist to support clinical and development programs in Verona, WI. The ideal candidate will have 8 years of experience in quality assurance, a BS/BA in a scientific field, and a thorough knowledge of drug GMP regulations. Responsibilities include reviewing vendor documentation, collaborating with various teams, and maintaining compliance with quality agreements. Competitive salary and excellent benefits offered. Applicants must be authorized to work in the US.

Qualifications

• 8 years of quality assurance experience in a pharmaceutical development setting.
• Excellent written and verbal communication skills with internal and external contacts.
• Ability to manage priorities independently in a fast-paced environment.

Responsibilities

• Provide quality assurance support to development and clinical programs.
• Review vendor documentation and perform lot disposition as per agreements.
• Collaborate with various departments for quality support.

Skills

Quality assurance

Communication skills

GMP regulations knowledge

Team player

Detail-oriented

Education

BS/BA in Chemistry, Biology, or Biochemistry

Tools

Adobe Acrobat

Microsoft Office

SmartSheet

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

The purpose of this position is to provide quality assurance support to programs utilizing contract development, manufacturing, and testing organizations. The incumbent will review vendor documentation and perform lot disposition per applicable quality agreements as well as capture quality data and generate metrics for vendors. The incumbent will be expected to interact with internal departments as well as multiple contract organizations to support ongoing pre-clinical and clinical development programs at Arrowhead Pharmaceuticals, Inc.

Responsibilities

• Interact with personnel companywide to obtain the necessary information and details to provide quality assurance support of development, clinical, and commercial programs.
• Review and approve vendor generated documentation, including but not limited to, master and executed batch records, testing records, certificates of analysis (CoA), labels, protocols, and reports.
• Perform lot disposition and generate certificates of compliance (CoC) as necessary.
• Collaborate with vendors on quality events and non-conformances as outlined in the applicable quality agreement.
• Review and release of completed manufacturing batch documentation including Quality Control data and issuance of Certificates of Analysis.
• Organization and control of quality, compliance, and project related documentation.
• Maintain knowledge of current compliance expectations and regulations pertaining to drug development
• Collaborate with, and provide quality support for, other departments (QC, Project Management, Toxicology, Clinical Operations, Supply Chain, etc.)
• Participate in meetings with vendors and external organizations as the QA team representative.
• Other duties consistent with the position as assigned from time to time.
• Assist with tracking vendor quality metrics; notify QA management of any performance issues.
• Assist with preparation, update, review, and routing of Arrowhead procedural documents.
• Draft, review, and approve standard operating procedures (SOP) and work instructions (WI) as needed.
• Assist with QA duties as needed.

Requirements

• 8 years of quality assurance experience in a pharmaceutical development company and/or contract manufacturing organization.
• BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry
• Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents.
• Excellent written and verbal communication skills and ability to communicate with internal and external parties.
• Highly motivated team player willing to contribute to a growing pharmaceutical organization.
• Ability to work independently with minimal supervision and as well as manage priorities within a fast-paced environment.
• A detail-oriented self-starter who endeavors to anticipate and resolve problems and seeks opportunities to grow their role and responsibilities at Arrowhead

Preferred{{:}}

• Previous experience with quality systems supporting drug-device combination products per 21 CFR Part 3 and medical devices QSR per 21 CFR Part 820/ISO 13485 is preferred.
• Competent knowledge of and ability to use Adobe Acrobat, Microsoft Office programs, and SmartSheet.

Arrowhead provides competitive salaries and an excellent benefit package.

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