Artiva Biotherapeutics

Manufacturing Associate I-II

Artiva Biotherapeutics • $75K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant science or engineering discipline or equivalent experience.
  • Minimum 1 year of cGMP biologics or cell culture manufacturing experience, ideally in biotech or cell therapy.
  • Experience in aseptic gowning and ISO 7 cleanroom environments is preferred.
  • Familiarity with cell culture methodologies including large-scale bioreactors and bag systems.
  • Knowledge of cGMP regulations and FDA guidance for biologics and cell therapies.

Responsibilities

  • Execute GMO manufacturing processes including cell expansion, harvest, and fill-finish.
  • Perform Aseptic Process Validation and participate in annual qualification activities.
  • Maintain cGMP compliance by strictly following established standards and procedures.
  • Support the development of batch records, workflows, and SOPs per regulatory requirements.
  • Utilize cell culture expertise for media preparation and handling bioreactors.
  • Lead reviews to enhance operational efficiency, identify risks, and drive process improvements.
  • Assist in the management of equipment and process change controls.

Benefits

  • Beautiful facility with a collaborative and innovative working environment.
  • Comprehensive health benefits including Medical, Dental, and Vision.
  • 401(k) retirement plan to support long-term savings.
  • Paid Time Off (PTO) and company-paid holidays for work-life balance.
  • Employee Assistance Program (EAP) to support mental and emotional health.
  • Recognition program allowing points trade-ins for personal rewards.
Full Job Description
Join Artiva Biotherapeutics in San Diego and work directly on the manufacturing floor to produce our innovative, off-the-shelf cell therapies in a state-of-the-art cGMP facility. Apply your expertise across cell culture, aseptic processing, harvest and fill-finish, playing a direct role in advancing therapies for patients with autoimmune diseases. Summary The successful candidate will play a key role in the manufacturing of cell therapies internally at Artiva. He/ she will execute hands-on manufacturing processes to deliver new revolutionary therapeutics. The ideal candidate will demonstrate in-depth knowledge of cGMP compliance, strong hands-on laboratory skills and work in a high-performing team of manufacturing associates. Key Responsibilities - Execute GMO manufacturing operations including cell expansion, harvest, and fill-finish. - Perform Aseptic Process Validation and participate in annual aseptic qualification. - Follow cGMP standards and procedures to maintain compliance. - Support development of batch records, workflows, and SOPs in accordance with regulatory and GMP requirements. - Apply cell culture expertise to media/buffer preparation, cell passaging, bioreactor production, and harvesting. - Lead after-action reviews to improve operational efficiency and KPIs, identify process gaps/risks, and implement sustainable improvements. - Support equipment and process change controls through implementation. - Work in Grade B and Grade C cleanroom environments. - Perform hands-on manufacturing operations directly on the floor. Qualifications - Bachelor's degree in a relevant science or engineering discipline, or equivalent work experience. - Minimum 1 year of cGMP biologics or cell culture manufacturing experience; biotech or cell therapy experience preferred. - Preferred experience with: - Aseptic gowning and ISO 7 cleanroom manufacturing - Cell counting platforms - Cell culture and expansion using bag systems and single-use large-scale bioreactors; Sartorius experience a plus - Lentiviral transduction - Automated and manual cell harvesting/washing; LOVO experience a plus - Cell selection/depletion using Miltenyi CliniMACS Prodigy - Fill-finish and cryopreservation in bags and vials; M1 filler and AT-vial experience a plus - Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. - Innovative, adaptable, and able to apply best practices in a small, growing environment. - Self-motivated with strong ownership, organizational skills, and the ability to prioritize and deliver results on time. Working Conditions and Physical Requirements - Work with cells and cell lines of human origin. - Ability to stand and work gowned for prolonged periods. NO AGENCIES PLEASE 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: $75,000 - $105,000. 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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