Associate II, Quality Assurance Document Control
Employment type
Full-time
Work setting
On-site
Location
San Diego, CA
Schedule
Day shift
Posted
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Job overview
The Associate II, Quality Assurance Document Control role is onsite in San Diego, CA. Compensation is not specified. Artiva Biotherapeutics is a clinical-stage biotechnology company developing natural killer cell-based therapies for autoimmune diseases. The role supports Quality Assurance Operations by maintaining controlled documents, training records, labeling, logbooks, and quality records. Accurate, traceable records and effective eQMS administration help sustain compliant quality systems and inspection readiness.
What you'll do
- Review and route document change requests
- format, track, and release controlled documents
- support electronic Quality Management System administration
- maintain training curricula, plans, and records
- coordinate controlled drug product labeling
- issue controlled documents and logbooks
- maintain paper and electronic records
- support audits and inspection readiness
- monitor periodic document reviews
- guide document authors and reviewers.
What we're looking for
- Skills & competencies
- quality assurancedocument controleqmsgmptraining recordscontrolled labelingrecords managementaudit supportsan diego caartiva biotherapeuticsbiotechnology
- Work arrangement
- Weekend coverage required
Why this role
The posting seeks 3+ years of experience in an FDA-regulated industry and a solid background in document control.
About the employer
Artiva Biotherapeutics is hiring for this role. Industry: Biological Product (except Diagnostic) Manufacturing. Sector: 32.
Additional details
- Industry sector
- 32
- Industry
- Biological Product (except Diagnostic) Manufacturing
- Occupation code
- 13-1041.00
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Listing ID: 4e87e5e8-eb0b-4958-a770-bedc5121fa29