QC Biology Associate II – Cell Therapy, cGMP

Artiva Biotherapeutics; San Diego (CA); In loco; USD 74.000 - 85.000; Tempo pieno

Descrizione del lavoro

Artiva Biotherapeutics is seeking a QC Associate II, QC Biology (Temporary) to perform routine cGMP release and stability testing of NK cell therapy products. You will support investigations, write reports, and help improve QC systems under supervision.

The role requires a BS/BA in biology or related field and at least 2 years of cGMP QC experience in a biotech/pharmaceutical setting. Base salary ranges from $74,000 to $85,000 annually.

Competenze

• Minimum 2 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting.
• Strong documentation practice and ability to write deviations and OOS investigations.
• Knowledge of method transfers, validations, and regulatory guidance interpretation.

Mansioni

• Assist in ordering supplies, reagents and equipment.
• Write and revise SOPs/Test methods that support Artiva’s cell therapy products.
• Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
• Support activities for QC equipment IQ/OQ/PQs.
• Perform routine cGMP release and stability testing of Artiva’s products; including biological tests, biochemistry, chemistry-based tests as needed.
• Support and as needed evaluate QC systems and/or implement system improvements with supervision.
• Support laboratory investigations and write reports for deviations and Out of Specification results.
• Document lab work in a thorough and accurate manner.

Conoscenze

cGMP QC experience

Technical writing

Critical thinking

Microsoft Word / Excel

Formazione

Bachelor’s degree in Biology or related field

Strumenti

ELISA

Flow Cytometry

Automated cell counters

IQ/OQ/PQ

Microsoft Word

Microsoft Excel

Descrizione del lavoro

Artiva Biotherapeutics is seeking a QC Associate II, QC Biology (Temporary) to perform routine cGMP release and stability testing of NK cell therapy products. You will support investigations, write reports, and help improve QC systems under supervision.

The role requires a BS/BA in biology or related field and at least 2 years of cGMP QC experience in a biotech/pharmaceutical setting. Base salary ranges from $74,000 to $85,000 annually.