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How much do artiva jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for artiva in the United States is $27.31, according to ZipRecruiter salary data. Most workers in this role earn between $21.39 and $31.25 per hour, depending on experience, location, and employer.

What is an Artiva?

An Artiva job typically refers to a role involving the Artiva software platform, which is used for account management, collections, and customer service operations. These positions are commonly found in industries like finance, healthcare, and call centers, where professionals use Artiva to manage accounts, automate workflows, and improve communication with clients. Responsibilities may include processing payments, managing customer interactions, and ensuring compliance with company policies.

What are typical daily responsibilities for an Artiva Collections Specialist?

As an Artiva Collections Specialist, your daily responsibilities include contacting customers by phone or email to resolve delinquent accounts, negotiating payment plans, and updating client records in the Artiva software system. You’ll also prepare and send collection notices, document all interactions with clients, and follow up on payment commitments. Collaboration with billing, customer service, and legal teams is common to ensure accounts are handled efficiently and in compliance with company policies. This dynamic role requires a balance of independent task management and teamwork for successful account resolution.

What are the key skills and qualifications needed to thrive in the Artiva position, and why are they important?

To excel as an Artiva Collections Specialist, you should have a solid understanding of accounts receivable processes, collections protocols, and customer account management, usually supported by relevant experience or education in finance or business. Familiarity with Artiva collection software, databases, and common office tools like Excel is highly valued, and certification in debt collection can be beneficial. Strong communication, negotiation skills, and the ability to remain patient and professional under pressure set top performers apart. These skills are crucial for efficiently recovering outstanding debts while maintaining positive client relationships and meeting compliance standards.

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Artiva jobs near you
Infographic showing various Artiva job openings in the United States as of August 2026, with employment types broken down into 97% Full Time, 2% Temporary, and 1% Contract. Highlights an 74% Physical, 2% Hybrid, and 24% Remote job distribution, with an average salary of $56,798 per year, or $27.3 per hour.

Supervisor, Quality Control Biology

Artiva Biotherapeutics

San Diego, CA • On-site

$135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Job description

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.


Job Summary:

Artiva Biotherapeutics is seeking a skilled and motivated Quality Control Supervisor who will be reporting to the Senior Manager, Quality Control. This individual will supervise the Bio Team and support QC biology testing. The individual will additionally perform routine cGMP release and stability testing of Artiva’s products.

Duties/Responsibilities:

  • Write and revise SOPs/Test methods that support Artiva’s cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Serve as primary QC Biology point of contact for cross-functional teams including Manufacturing, QA, and Regulatory Affairs for release and investigation activities.
  • Lead training and qualification of Bio team members on equipment use and biological test methods.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Lead and perform routine cGMP release and stability testing of Artiva’s products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Lead evaluation of QC systems and/or implementation of system improvements.
  • Perform laboratory investigations and write reports for deviations.
  • Ensure data integrity practices (ALCOA+ principles) are followed by the Bio team; support LIMS/ELN implementation and administration as applicable.
  • Assist in laboratory investigations for Out of Specification results.
  • Assist in biological method qualification and validation as needed.
  • Perform periodic trending of QC testing data; identify adverse trends and initiate CAPAs as appropriate.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Planning and scheduling for GMP in-process and release testing.
  • Reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist QC and AD team for analytical qualification and validation, as necessary.
  • Develop an in-depth understanding of NK and CAR-NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.

Qualifications:

  • Bachelor’s degree (BS/BA) in Biology, Biochemistry, Immunology, or a related life science field required.
  • Experience with NK cell or CAR-modified cell therapy products preferred; familiarity with viability, cytotoxicity, identity, and potency assays for cell therapy products.
  • Minimum 8 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • At least 1 year of Supervisory or team lead experience is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and strong experience with guidance interpretation and application
  • Excellent critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word, Project, Visio, and Excel programs.


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!

Base Salary: $ 110,000 - $135,000. Exact compensation may vary based on level, skills and experience.