Backed by 5AM Ventures.
About the role
Artiva Biotherapeutics is an equal employment opportunity employer.
What they're looking for
- Solid background in document control , prior experience working with electronic quality management systems preferred
- 3+ years’ experience in an FDA regulated industry
- Strong Proficiency in MS Office applications
- Able to lift boxes weighing up to 30 lbs
- Strong communication skills (verbal & written) including ability to interact positively with all levels of the organization
- Ability to work independently
More about this role
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, create an opportunity to generate potentially transformative therapies.
For more information, visit www.artivabio.com
We’re seeking a QA Document Control professional with 3+ years of GMP/regulatory experience to manage:
- Document lifecycle from redlines to document release
- Support LMS administration and training compliance
- Assist with administration of the electronic Quality Management System
- Contribute to site records management and inspection readiness activities
- Bring strong attention to detail, ownership, and a hands-on approach to Quality.
Overview
This position is...
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