Associate Director, Clinical Quality Assurance

🔥 0 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $172k - $195k / year

⏰ Full Time

🟠 Senior

🔧 QA Engineer (Quality Assurance)

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Artiva Biotherapeutics

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51 - 200 employees

💰 Series B on 2021-02

Artiva Biotherapeutics is an immunotherapy company with the ability to produce off-the-shelf, allogeneic NK cell therapies at a massive scale. Our mission is to develop effective, safe and accessible cell therapies for patients with devastating autoimmune diseases and cancers. Our lead program, AlloNK®, is an allogeneic, non-genetically modified NK cell therapy candidate designed to enhance the activity of monoclonal antibodies or NK cell engagers. AlloNK is currently in clinical trials in combination with rituximab for treatment of systemic lupus erythematosus (SLE) in patients with active lupus nephritis and for treatment of Non-Hodgkin Lymphoma, as well as in combination with Affimed’s innate cell engager AFM13 for the treatment of patients with relapsed/refractory CD30-positive lymphomas.

📋 Description

• Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across all phases of clinical development • Develop, implement and conduct risk-based GCP quality oversight strategies • Lead investigations of significant GCP quality and compliance events • Plan, conduct, and manage audits of clinical investigator sites, CROs, vendors • Maintain required documentation and quality records in accordance with Artiva procedures • Lead inspection readiness activities for assigned programs and support regulatory authority inspections • Interact with internal teams to ensure quality compliance across all aspects of clinical development • Define and implement a strategy to review key regulatory documents • Lead development and implementation of clinical quality procedures in collaboration with Clinical Development

🎯 Requirements

• BS or BA in a scientific field • 8+ years of clinical and/or QA experience in biologics or pharma • 4+ years of Clinical QA experience • Knowledge and hands on experience in regulatory inspections, clinical investigator site/vendor/internal audits • Thorough knowledge of current Good Clinical Practices and Good Clinical Laboratory Practices as they relate to all phases of cell therapy product human clinical trials. • Expert level of understanding of CLIA and CAP. • Knowledge of ICH, GCP, GCLP, Data Privacy and other applicable regulations and requirements in the pharmaceutical/biopharma industry. • Computer skills required to operate Microsoft Word, Project, and Excel programs.

🏖️ Benefits

• Medical, Dental, and Vision • Group Life Insurance • Long Term Disability (LTD) • 401(k) Retirement Plan • Employee Assistance Program (EAP) • Flexible Spending Account (FSA) • Paid Time Off (PTO) • Company paid holidays, including the year-end holiday week • Recognition program, Bonus.ly, to trade in points for rewards