Cell Therapy Process Development Engineer Onsite Contract

Pyramid Consulting, Inc; Los Angeles (CA); On-site; USD 143,270,000 - 146,136,000; Full time

Job summary

Pyramid Consulting, Inc. is actively seeking a Cell Therapy Process Development Manufacturing Engineer for a 6+ month onsite contract in Los Angeles, CA.

The role focuses on hands-on cell culture and aseptic processing within ISO 5 environments, employing automated platforms and DOE-driven process optimization. The engineer will contribute to tech transfer and GMP manufacturing support, collaborating with cross-functional teams.

Qualifications

• MS in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or related field with 2+ years of relevant pharmaceutical/biotechnology manufacturing and process development experience; or
• BS in a related engineering/biotechnology discipline with 4+ years of relevant experience
• AS in a related discipline with 5+ years of relevant experience; or
• High School Diploma with 6+ years of relevant pharmaceutical/biotechnology manufacturing and process development experience.

Responsibilities

• Design and execute cell therapy process development experiments using automated platforms.
• Perform hands-on laboratory work in a cell culture environment.
• Execute aseptic processing activities in an ISO 5 environment.
• Develop, optimize, and characterize processes supporting autologous T-cell therapies.
• Evaluate new technologies, materials, equipment, and process improvements for GMP manufacturing.
• Apply Design of Experiments (DOE) and statistical analysis to process development studies.

Skills

Cell therapy

Process development

Automated platforms

DOE/Statistics

JMP/Minitab

cGMP/GMP

Flow cytometry

MRNA handling

Bioreactors/Scale-up

Education

MS in Biochemical/Chemical/Biomedical Engineering

BS in related engineering/biotech with 4+ years

AS with 5+ years

HS with 6+ years

Tools

JMP

Minitab

Job description

Pyramid Consulting, Inc. is actively seeking a Cell Therapy Process Development Manufacturing Engineer for a 6+ month onsite contract in Los Angeles, CA.

The role focuses on hands-on cell culture and aseptic processing within ISO 5 environments, employing automated platforms and DOE-driven process optimization. The engineer will contribute to tech transfer and GMP manufacturing support, collaborating with cross-functional teams.