Senior Associate, QA Compliance

Artiva Biotherapeutics

San Diego, California, United StatesFull-timePosted 2mo ago

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About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.


For more information, visit www.artivabio.com.


This position is responsible for Quality Assurance Compliance activities supporting deviations, CAPAs, change control, and product releases.


Duties/Responsibilities:

 

  • Support the deviation and CAPA/SCAR Systems by investigating, reviewing, assessing, tracking, follow-up, and completing all quality events.
  • Support the Change Control program by reviewing, assessing, tracking, follow-up, and completing all change control documentation.
  • Maintain databases and metrics.
  • Identify and communicate compliance gaps; propose phase appropriate solutions.
  • Track the status of Deviations, CAPAs, and Change Controls.
  • Perform internal and/or external audits, as needed.
  • Support product releases by reviewing batch records.
  • Support risk assessment activities.
  • Support audits by regulatory or state agencies and partners.
  • Follow applicable regulations, including FDA, ISO, ICH, and company policies and procedures.
  • Support other QA department needs as identified by management.


Requirements:


  • Bachelor’s degree or a combination of relevant education and applicable job experience
  • 5+ years’ experience in an FDA regulated industry and CGMP regulations.
  • Late-phase to commercial phase experience a plus.
  • Cell Therapy experience a plus.


In addition to a great culture, we offer:

  • A beautiful facility 
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • 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
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.


If all this speaks to you, come join us on our journey!

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Frequently asked questions

Who is hiring for Senior Associate, QA Compliance at Artiva Biotherapeutics?+
Artiva Biotherapeutics is actively hiring for this Senior Associate, QA Compliance role. Click "Apply Now" to submit your application directly on Artiva Biotherapeutics's careers page — Careeronaut doesn't charge employers or candidates for referrals.
When was this Senior Associate, QA Compliance role posted?+
This listing was first posted on 2026-06-16. We pull the latest copy from the source feed daily, and any role that's taken down gets removed from Careeronaut within seven days so you don't waste time on stale listings.
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