Arrowhead Pharmaceuticals, Inc.
Director, Quality Assurance (Combination Products)
Arrowhead Pharmaceuticals, Inc., San Diego, California, United States, 92189
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
The purpose of this position within the Quality and Compliance department is to quality leadership and oversight of medical device / drug combination products development and management at Arrowhead.
This position will report to the Vice President Quality and Compliance and work closely with members of the Operations, Supply Chain, Regulatory, Quality, and Commercial teams, as well as external stakeholders and suppliers to support Quality Management System (QMS) and ensure the clinical and commercial presentations of combinational product quality and compliance with relevant laws and company's strategic goals.
Responsibilities
Serve as an internal subject matter expert in the combinational products and primary lead for all relevant elements of QMS and quality aspects of the combinational product development and managementMonitor, guide, and ensure internal stakeholders' decision-making and actions are consistent with cGMPs, QSR, ISO 13485, Good Distribution Practices (GDP), relevant international laws and guidances, and Arrowhead policies and proceduresDevelop and maintain quality strategy and provide quality guidance to engineering team during all phases of design control, risk management, human factor engineering, process development, verification/validation testing, packaging, and distribution, as well as lifecycle management of design changes and documentationEstablish and maintain electronic Design History File (DHF) and Device Master File (DMF), and relevant to the combinational product elements of QMSChampion, maintain, and support continuous improvement to the combination product QMS, monitor and identify areas for improvement and ensure remediationSupport development and management of Quality Agreements, external audits of suppliers, and 3rd parties within the Supply ChainSupport internal audits, certifications, and facilitate regulatory inspections at Arrowhead and it's suppliersPrepare and present to management periodic reports and status of regulatory compliance of combination product, QMS, DMF, including the measures and activities to ensure complianceOther duties as assignedRequirements:
BS or BA Degree in relevant scientific or engineering discipline, and at least 8 years of relevant experienceStrong knowledge of FDA regulations (21 CFR Part 820, 21 CFR Parts 210/211), ISO 13485, and other relevant international standardsExperience leading QMS implementation, maintenance, and improvement initiatives, including CAPA, change control, and risk management processesExperience in engaging with regulatory authoritiesCompetent knowledge of and ability to use Microsoft Office suitePrior experience with use of an electronic document management system in a regulated environmentAbility to follow company procedures, work instructions, and policiesAbility to process, synthesize and summarize complex issuesExcellent judgment, and analytical, problem-solving skillsWork in a safe manner; properly handle materials and chemicalsExcellent attention to detail and organizational skillsAbility to multi-task and prioritize work tasks with minimal supervisionExcellent interpersonal, verbal, and written communication skillsPreferred:
Master's degreeRelevant professional certification
California pay range
$180,000-$225,000 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
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
The purpose of this position within the Quality and Compliance department is to quality leadership and oversight of medical device / drug combination products development and management at Arrowhead.
This position will report to the Vice President Quality and Compliance and work closely with members of the Operations, Supply Chain, Regulatory, Quality, and Commercial teams, as well as external stakeholders and suppliers to support Quality Management System (QMS) and ensure the clinical and commercial presentations of combinational product quality and compliance with relevant laws and company's strategic goals.
Responsibilities
Serve as an internal subject matter expert in the combinational products and primary lead for all relevant elements of QMS and quality aspects of the combinational product development and managementMonitor, guide, and ensure internal stakeholders' decision-making and actions are consistent with cGMPs, QSR, ISO 13485, Good Distribution Practices (GDP), relevant international laws and guidances, and Arrowhead policies and proceduresDevelop and maintain quality strategy and provide quality guidance to engineering team during all phases of design control, risk management, human factor engineering, process development, verification/validation testing, packaging, and distribution, as well as lifecycle management of design changes and documentationEstablish and maintain electronic Design History File (DHF) and Device Master File (DMF), and relevant to the combinational product elements of QMSChampion, maintain, and support continuous improvement to the combination product QMS, monitor and identify areas for improvement and ensure remediationSupport development and management of Quality Agreements, external audits of suppliers, and 3rd parties within the Supply ChainSupport internal audits, certifications, and facilitate regulatory inspections at Arrowhead and it's suppliersPrepare and present to management periodic reports and status of regulatory compliance of combination product, QMS, DMF, including the measures and activities to ensure complianceOther duties as assignedRequirements:
BS or BA Degree in relevant scientific or engineering discipline, and at least 8 years of relevant experienceStrong knowledge of FDA regulations (21 CFR Part 820, 21 CFR Parts 210/211), ISO 13485, and other relevant international standardsExperience leading QMS implementation, maintenance, and improvement initiatives, including CAPA, change control, and risk management processesExperience in engaging with regulatory authoritiesCompetent knowledge of and ability to use Microsoft Office suitePrior experience with use of an electronic document management system in a regulated environmentAbility to follow company procedures, work instructions, and policiesAbility to process, synthesize and summarize complex issuesExcellent judgment, and analytical, problem-solving skillsWork in a safe manner; properly handle materials and chemicalsExcellent attention to detail and organizational skillsAbility to multi-task and prioritize work tasks with minimal supervisionExcellent interpersonal, verbal, and written communication skillsPreferred:
Master's degreeRelevant professional certification
California pay range
$180,000-$225,000 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