Senior Flow Cytometry & Cell Therapy Analytics Lead

F. Hoffmann-La Roche AG

South San Francisco (CA)

On-site

USD 147,000 - 272,000

Full time

5 days ago
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Benefits offered by this job

Relocation benefits
Discretionary annual bonus

Job summary

Genentech, part of the Roche group, seeks a highly experienced leader to head flow cytometry analytical development for cell therapy programs in South San Francisco. You will guide method development, tech transfer, and cross-functional collaboration to ensure analytical readiness across CMC and regulatory milestones.

The role requires a PhD with extensive relevant experience or a MS/BS with senior-level responsibilities, strong QbD knowledge, and hands-on cytometry expertise.

Qualifications

  • PhD with 3+ years in biotech/pharma, preferably cell therapy.
  • Experience supervising analytical development teams.
  • Strong knowledge of QbD, cGMPs, ICH, and FDA.
  • Hands-on with multicolor flow cytometry and cell-based assays.

Responsibilities

  • Provide technical leadership for flow cytometry method development.
  • Represent analytical development in CMC and program meetings.
  • Oversee technology transfer to GMP QC and external partners.
  • Collaborate across functions to support method development and product characterization.
  • Mentor and train teams on flow cytometry methods.
  • Stay updated on industry trends and analytical platforms.
  • Draft reports, SOPs, and test protocols.
  • Guide the team to meet key program milestones.

Skills

Flow cytometry
Cell-based assays
QbD principles
DOE
CMC documents
Mentoring
Statistical methods
Cross-functional lead

Education

Ph.D. in Biological Sciences or related field
MS/BS considered

Tools

qPCR
ddPCR
ELISA
NGS

Job description

Genentech, part of the Roche group, seeks a highly experienced leader to head flow cytometry analytical development for cell therapy programs in South San Francisco. You will guide method development, tech transfer, and cross-functional collaboration to ensure analytical readiness across CMC and regulatory milestones.

The role requires a PhD with extensive relevant experience or a MS/BS with senior-level responsibilities, strong QbD knowledge, and hands-on cytometry expertise.

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