About Artiva:
Artiva is clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers.
Artiva’s lead product candidate, AlloNK, is a non-genetically modified, off-the-shelf, allogeneic, cryopreserved NK cell therapy designed to enhance the antibody-dependent cellular cytotoxicity (ADCC) effect of mAbs to drive B-cell depletion and to be administered in the community setting. Unlike CAR-T and any genetically modified cell therapy, AlloNK is a non-genetically modified NK cell therapy candidate and has not shown any secondary malignancies in our clinical trials, which is a benefit in an autoimmunity setting. Using the company’s proprietary cell therapy manufacturing platform, Artiva can generate thousands of doses of cryopreserved, infusion-ready AlloNK cells from a single cord blood unit. The FDA has granted Fast Track designation to AlloNK in combination with rituximab or obinutuzumab for the treatment of class III or IV lupus nephritis, and AlloNK in combination with rituximab for the treatment of relapsed or refractory non-Hodgkin lymphoma of B-cell origin (B-NHL).
AlloNK, is currently being evaluated in combination with B-cell targeted mAbs in
patients with autoimmune diseases and cancers, such as lupus nephritis, SLE, rheumatoid arthritis, pemphigus vulgaris, the ANCA-associated vasculitis subtypes GPA/MPA, and B-NHL. In addition, we are also pursuing AlloNK and our CAR-NK product candidates in multiple indications through collaborator-funded trials. Artiva’s cell therapy manufacturing platform incorporates cell expansion and activation technology developed by Artiva’s strategic partner, GC Cell Corporation, a member of the GC family of companies, a leading healthcare company in Korea.
Artiva is headquartered in San Diego and backed by leading venture investors including 5AM Ventures, RA Capital Management and venBio Partners.
For more information, visit www.artivabio.com.
Job Summary:
The Materials Management & Logistics Associate III works with procurement, inventory, receipt and release of manufacturing and QC materials for our newly established manufacturing facility. This position works closely with Manufacturing and QC, and QA teams from Technical Operations as well as corporate procurement to understand their needs and priorities. This position also schedules all product shipments between CMO, Storage Depot, and Artiva while maintaining all appropriate customs documentations as required.
Duties and Responsibilities:
- Assist in development and implementation of materials management and supply chain processes
- Perform daily supply chain operations including shipping, receiving, record keeping/documentation, inventory management, and order processing of all materials for Artiva manufacturing and QC operations
- Assist in development and implementation of manufacturing materials kitting as needed
- Proficiency in ERP and paper-based receiving/inventory systems
- Maintain accurate records of receipt and release of materials
- Perform inventory count of materials as needed
- Assist with development and modification of SOP’s for supply chain/materials management processes as needed
- Ensure that all documentation and materials transactions are completed accurately and following Good Documentation Practices
- Preparation of outbound shipments, including preparation of records and preparation of goods for final shipment as needed
- Coordinate shipment schedules with specialty couriers and preparation of international shipping documentations
- Lead efforts in resolving shipping issues related to international customs delays.
- Collaborate with internal departments to ensure proper shipping of regulated and non-regulated materials, work with external shipping agents and vendors to resolve issues as needed
- Perform reconciliation of order discrepancies and following up with purchasing, vendors and end users as needed
- Create purchase requisition requests to meet operational needs
- Adhere to appropriate PPE and safety rules
- Assist in all other materials management and supply operations deemed necessary to complete organizational goals.
Requirements:
- A minimum of 4 years of experience in a regulated shipping and receiving/materials management position, preferably in biotech or life sciences
- Familiarity with GMP regulations as related to Pharma/Biotech/ industries preferred
- Cold chain experiences (2-8⁰C, -20⁰C, -80⁰C, and below -150⁰C).
- Strong attention to detail and problem-solving skills
- Proficient experience with ERP use and implementation a plus
- Proficiency in Microsoft Office and the ability to learn new applications quickly and easily
- Knowledge of various inventory management systems
- Good collaborative and team-oriented communication
- Experience in a start-up setting a plus
- Experience in a dynamic, fast paced, growing environment
- May need to work with hazardous materials
- Must be able to lift, carry, push and/or pull 50 pounds of equipment or supplies.
Why you should apply:
We have a fantastic team and philosophy! We are passionate – we deeply care about our team, our science, and improving the lives of patients. We are innovative - pushing into new frontiers for patient benefit. We are transparent - believers in flat, accessible, and open communication paths. We are inclusive – committed to the diversity of our team and ensuring that all voices are heard.
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: $41-45/hr. Exact compensation may vary based on skills and experience.
