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What is it like to work at Amgen?

Amgen is a biotechnology company that values innovation, collaboration, and patient-centricity, fostering a culture that encourages open communication and teamwork among its employees. The company's research and development teams work in a dynamic environment, often in collaboration with external partners and academia, to develop and deliver life-changing medicines to patients with serious diseases. Working at Amgen may appeal to candidates who are passionate about advancing medical science and improving human health, as the company offers opportunities for professional growth, mentorship, and contributions to groundbreaking research.

What makes Amgen an attractive place to work?

Amgen is a leading biotechnology company that has been at the forefront of innovation in the pharmaceutical industry for decades, with a strong focus on developing life-changing medicines for patients with serious diseases. The company's work environment is characterized by a culture of collaboration, innovation, and scientific excellence, with opportunities for employees to work on cutting-edge projects and contribute to groundbreaking research. As a result, Amgen offers a dynamic and challenging work environment that can provide employees with opportunities for professional growth, development, and impact in the field of biotechnology.

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Infographic showing various Senior Associate Quality Control job openings at Amgen in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% Physical, and 20% Remote job distribution.

Senior Associate, Quality Control, Raw Materials

Artiva Biotherapeutics, Inc.

San Diego, CA • On-site

$96K - $110K/yr

Full-time

Re-posted 4 hours 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 motived Senior Quality Control Associate who will be reporting to the Sr. Manager, Quality Control of Raw Materials. The Senior Associate of Raw Materials will support the qualification and release of raw materials used in GMP manufacturing by coordinating, reviewing, and approving analytical testing performed by contract testing laboratories. This role requires strong technical expertise in wet chemistry, HPLC, and mass spectrometry to critically review external laboratory data, assess suitability for use, and support investigations. The position serves as a key technical interface between internal Quality, Supply Chain, Manufacturing, and external contract laboratories. Experience with ATMPs and biologically derived raw materials is a strong plus.
Duties/Responsibilities:
  • Coordinate submission of raw material samples to qualified contract testing laboratories, including preparation of testing requests, timelines, and documentation
  • Serve as the primary QC point of contact for external laboratories performing raw material testing
  • Ensure testing is performed per approved specifications, compendial methods, and quality agreements
  • Perform technical review and approval of raw material test results generated by contract laboratories, with emphasis on: Wet chemistry data, HPLC chromatographic data and trends, Mass spectrometry-based identity and impurity assessments
  • Evaluate data for compliance with specifications, GMP requirements, and data integrity expectations
  • Identify atypical results, trends, or discrepancies and initiate follow up with vendors as needed
  • Support qualification and oversight of biologically derived raw materials commonly used in ATMP and cell therapy manufacturing (e.g., media components, cytokines, growth factors, enzymes)
  • Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications
  • Author, review, and approve GMP documentation including SOPs, test methods, protocols, reports, deviations, CAPAs and change controls
  • Maintainer accurate and compliant laboratory records in LIMS, ELN, and paper-based systems
  • Support internal, external, and regulatory audits (FDA, EMA, etc.)
  • Act as a subject matter expert (SME) for raw material testing methods and regulatory expectations
  • Troubleshoot assay failures, out-of-specification (OOS, and out-of-trend (OOT) results
  • Support method transfers, verifications, and validations for raw material assays
  • Evaluate supplier documentation including BSE/TSE, CoAs, COC, COI, technical packages, SDS and quality agreements
  • Identify opportunities to improve testing efficiency, data integrity, and compliance
  • Support implementation of new technologies, methods, and systems
  • Participate in cross-functional teams with QA, Manufacturing, Materials Management and Product Development
  • Support or lead QC special projects as needed

Qualifications:
  • Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or related scientific discipline.
  • 4+ years of experience in GMP QC or analytical roles, with demonstrated experience reviewing and approving external laboratory data.
  • Strong technical knowledge of wet chemistry testing principles, HPLC data interpretation and troubleshooting, Mass spectrometry (LC-MS or similar) concepts.
  • Experience of raw material testing requirements and regulatory expectations (USP, EP, ICH)
  • Experience with cell therapy-relevant materials (media, cytokines, sera, reagents, consumables)
  • Experience supporting material qualification and release through contract testing laboratories.
  • Solid understanding of GMPs, data integrity, and QC documentation practices.
  • 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.

If all this speaks to you, come join us on our journey!
Base Salary: $96,000 - $110,000. Exact compensation may vary based on skills and experience.

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