Senior MSAT Engineer – Process Transfer & GMP Excellence

Artiva Biotherapeutics Inc.

San Diego (CA)

Presencial

USD 150.000 - 165.000

Jornada completa

Hace 10 días
Generador de candidaturas

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Ventajas ofrecidas por este puesto de trabajo

Medical, Dental, Vision
401(k) Retirement Plan
Paid Time Off

Descripción de la vacante

Artiva Biotherapeutics Inc. is seeking a Sr. Manager, MSAT Engineer to drive tech transfer, validation, and manufacturing excellence for NK cell therapies. You will support clinical and commercial manufacturing, write master batch records, SOPs, and risk assessments, and lead deviation investigations.

The role requires deep GMP knowledge, strong problem-solving skills, and experience with cGMP in regulated environments. Excellent collaboration and communication are essential.

Formación

  • Must hold Bachelor’s, Master’s, or PhD in biotechnology, chemical engineering, or related fields.
  • Experience managing complex MSAT projects in late-stage clinical/commercial manufacturing.
  • Strong ability to establish standardized processes and governance in regulated settings.

Responsabilidades

  • Lead tech transfer of new processes into the site.
  • Prepare documents to support validation and batch manufacturing.
  • Troubleshoot manufacturing processes and drive investigations.
  • Track/process deviations and CAPA implementation.
  • Create dashboards for manufacturing data visualization.

Conocimientos

Project management
Tech transfer
Process validation
Communication
Cell therapy
GMP / cGMP
Problem solving

Educación

Bachelor’s/Master’s/PhD in biotech or chemical engineering

Herramientas

IQ/OQ/PQ
CAPA

Descripción del empleo

Artiva Biotherapeutics Inc. is seeking a Sr. Manager, MSAT Engineer to drive tech transfer, validation, and manufacturing excellence for NK cell therapies. You will support clinical and commercial manufacturing, write master batch records, SOPs, and risk assessments, and lead deviation investigations.

The role requires deep GMP knowledge, strong problem-solving skills, and experience with cGMP in regulated environments. Excellent collaboration and communication are essential.

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