Senior MSAT Engineer, Cell Therapy Manufacturing

Artiva Biotherapeutics; San Diego (CA); On-site; USD 150,000 - 165,000; Full time

Benefits offered by this job

Medical, Dental, and Vision

401(k) Retirement Plan

Paid Time Off (PTO)

Year-end holiday week

Job summary

Artiva Biotherapeutics is seeking a Sr. Manager, MSAT Engineer to lead technical transfer and support for clinical and commercial NK cell manufacturing.

You will drive process validation, batch records, deviations investigations, CAPA programs and data trending in a cGMP environment. Join a fast-paced, collaborative MSAT team focused on scalable manufacturing and cross-functional partnerships, contributing to the development of AlloNK therapies.

Qualifications

• Bachelor’s, Master’s or PhD in biotechnology, chemical engineering or related disciplines.
• Proven experience in managing complex projects.
• Technical depth & process expertise in late-stage clinical and commercial manufacturing.
• Ability to establish business processes, drive standardization and governance in complex environments.

Responsibilities

• Provides technical assistance for process tech transfer and validation efforts for assigned manufacturing projects.
• Writes Master Batch Records, SOPs, deviation reports and technical risk assessment with a strong understanding of equipment, process and testing.
• Lead deviations process under QA supervision and performs thorough Root Cause Analysis.
• Monitors manufacturing processes during production runs to assess any technical process issues and provides troubleshooting support as needed.
• Author manufacturing investigations and drives CAPA implementation.
• Support raw materials characterization and E&L risk assessment.
• Creates dashboard to visualize manufacturing
• Other duties as assigned.

Skills

Process transfer

CAPA & RCA

cGMP manufacturing

Project management

Cell therapy manufacturing

Education

Biotech/Engineering degree

Job description

Artiva Biotherapeutics is seeking a Sr. Manager, MSAT Engineer to lead technical transfer and support for clinical and commercial NK cell manufacturing.

You will drive process validation, batch records, deviations investigations, CAPA programs and data trending in a cGMP environment. Join a fast-paced, collaborative MSAT team focused on scalable manufacturing and cross-functional partnerships, contributing to the development of AlloNK therapies.