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Job description
Artiva Biotherapeutics seeks a skilled QC Associate I or II for Environmental Monitoring (Contract to hire) to support the Quality Control EM program and report to the Manager, Quality Control. This role monitors the cGMP manufacturing environment to detect potential contaminants and assists in growth promotion testing of media used in biopharmaceutical manufacturing.
Requirements include a BA/BS in Microbiology and 1–3 years of cGMP QC experience in biotech/pharma, with aseptic techniques and
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.