Artiva Biotherapeutics

Associate II, Quality Control Biology

Artiva Biotherapeutics$79K — $91K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in biology or related field required.
  • Minimum of 2 years of cGMP QC experience in cell therapy, biotech, or pharmaceuticals.
  • Familiarity with cGMP deviations and Out of Specifications (OOS) management.
  • Basic knowledge of method transfers and qualifications in QC processes.
  • Proficient in Microsoft Word and Excel, with a focus on technical writing and critical thinking.

Responsibilities

  • Assist in ordering laboratory supplies and equipment for testing.
  • Write and revise Standard Operating Procedures (SOPs) and test methods.
  • Operate ELISA, Flow Cytometers, and other analytical instruments for testing.
  • Perform routine cGMP release and stability testing for NK cell therapy products.
  • Support laboratory investigations and respond to deviations and OOS results.
  • Document lab activities thoroughly in compliance with company policies.
  • Contribute to continuous improvement of QC systems and methods.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • Group life insurance and long-term disability coverage.
  • 401(k) retirement plan with company matching.
  • Employee Assistance Program (EAP) for personal support.
  • Flexible Spending Account (FSA) for medical expenses.
  • Generous paid time off and company holidays.
  • Access to a recognition program that rewards employee achievements.
Full Job Description
Job Summary: Artiva Biotherapeutics is seeking a skilled and motived QC Associate II, QC Biology who will be reporting to the Senior Manager, Quality Control. This individual will perform routine cGMP release and stability testing of Artiva's NK cell therapy products, support laboratory investigations, and contribute to continuous improvement of QC systems. Duties/Responsibilities: - Assist in ordering supplies, reagents and equipment. - 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. - Support activities for QC equipment IQ/OQ/PQs. - Perform routine cGMP release and stability testing of Artiva's products; including biological tests, biochemistry, chemistry-based tests as needed. - Support and as needed evaluate QC systems and/or implement system improvements with supervision. - Support laboratory investigations and write reports for deviations and Out of Specification results. - Document lab work in a thorough and accurate manner. - Perform all work according to company policies, SOPs, and cGMP practices. - Assist in planning for GMP release testing, including testing schedules, reviewing biology data and investigating OOS and OOT results. - Write technical QC protocols and reports as needed. - Assist in analytical qualification and validation, as necessary. - Support the transfer and optimization of analytical methods from Analytical Development (or contract laboratories). - Develop an in-depth understanding of NK products, testing, and safety. - Maintain records and databases in accordance with procedures. - Support other special QC projects as needed. Qualifications: - Bachelor's degree (BS/BA) or relevant scientific field, preferably in biology or related field. - Minimum 2 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required. - Knowledge and experience in supporting cGMP deviations, OOS, etc. - Basic knowledge of method transfers, qualifications, and validations; current industry practices; and some experience with guidance interpretation and application - Adept at learning critical thinking and technical writing skills. - Computer skills required to operate Microsoft Word 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. Base Salary: $ 79,000 - $ 91,000. Exact compensation may vary based on level, skills and experience.

About Artiva Biotherapeutics

Artiva Biotherapeutics is a clinical-stage biotechnology company developing a pipeline of novel, precisely targeted immuno-oncology therapies. The company's proprietary technology platform leverages a deep understanding of the biology of immune cells and their interactions with cancer cells to develop therapies that can selectively activate or suppress immune responses to cancer. Artiva's lead product candidate, AB-101, is a first-in-class, off-the-shelf, allogeneic cell therapy that targets solid tumors by activating natural killer (NK) cells. The company was founded in 2019 and is headquartered in South San Francisco, California.
Learn more about Artiva Biotherapeutics
Size
20 employees
Industry
Net Income
-$16
Founded
2019
NASDAQ

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