Cell Therapy Process Engineer II

Spectraforce Technologies; San Mateo (CA); On-site; USD 110,000 - 140,000; Full time

Job summary

Spectraforce Technologies is seeking a Process Engineer II to advance cell therapy process development, design and execute experiments, and support technology transfer within GMP manufacturing environments.

The role requires hands-on lab work, data analysis, protocol drafting, and collaboration with research, development, and manufacturing teams to drive process improvements and regulatory documentation.

Qualifications

• MS/BS/AS in biochemical/chemical/biomedical engineering or related with pharma/manufacturing process development.
• 2+ years (MS) or 4+ years (BS) or 5+ years (AS) of pharma/manufacturing process development.
• Experience with automated cell therapy platforms and aseptic processing.

Responsibilities

• Design and execute cell therapy process development experiments on automated platforms.
• Lead technology transfer and support GMP manufacturing operations.
• Analyze data, draft protocols, SOPs, and batch records.
• Provide training to GMP manufacturing personnel and communicate results to stakeholders.
• Present results to cross-functional teams and leadership.

Skills

Automated platforms

Cell culture techniques

cGMP manufacturing

Design of Experiments

Statistical analysis

Problem solving

Communication

Independent worker

Team collaboration

Flow cytometry knowledge (plus)

mRNA handling knowledge (plus)

Education

MS in Biochemical/Chemical/Biomedical Engineering or related

BS in Biochemical/Chemical/Biomedical Engineering or related

AS in Biochemical/Chemical/Biomedical Engineering or related

High School + 6+ years pharma/manufacturing experience

Tools

JMP

Minitab

Job description

Spectraforce Technologies is seeking a Process Engineer II to advance cell therapy process development, design and execute experiments, and support technology transfer within GMP manufacturing environments.

The role requires hands-on lab work, data analysis, protocol drafting, and collaboration with research, development, and manufacturing teams to drive process improvements and regulatory documentation.