Senior Scientist, Analytical Operations — QC & Partnerships

Dispatch Biotherapeutics, Inc.

Philadelphia (Philadelphia County)

On-site

USD 120,000 - 170,000

Full time

7 days ago
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Benefits offered by this job

Equity
Medical coverage
401(k)
Life insurance
Flexible PTO
Other benefits

Job summary

Dispatch Biotherapeutics, Inc. is seeking a Senior Scientist to support Analytical Operations for our portfolio of product candidates, including viral vectors and CAR T cells. You will build and manage an efficient operational network, coordinate external testing with CDMOs, and ensure high-quality data generation and method transfer activities.

The role requires a Ph.D. with 5+ years or equivalent industry experience, strong GMP/GLP familiarity, and excellent collaboration across internal teams

Qualifications

  • Ph.D. with at least 5 years of related experience in an industry setting
  • Master’s Degree with at least 8 years of related experience in an industry setting
  • Bachelor’s Degree with at least 10 years of related experience in an industry setting
  • CMC analytical experience within cell and gene therapy and/or large molecule antibody therapy
  • Experience with method development, validation, and method transfers in accordance with ICH guidelines
  • Lab-based experience developing methods and performing routine testing on cell-based, Flow Cytometry, qPCR, ddPCR, etc.
  • Experience scheduling testing for a team (lab-based scheduling of analysts, manufacturing-based scheduling of operators)
  • Experience as a lab manager: ordering supplies and organizing reagents
  • Experience using electronic lab notebook (ELN) systems (Symyx, Benchling, etc.)
  • Experience with data analysis software such as GraphPad Prism, JMP, and Microsoft Excel
  • Experience shipping samples domestically and internationally
  • Highly organized and proactive in setting up systems for data capture and tracking
  • Experience working in a cross-functional matrix team
  • Strong attention to detail and accurate documentation of data
  • Experience collaborating with external partners (CDMOs and CTLs) and internal cross-functional teams
  • Effective oral and written communication skills
  • Familiarity with GMP/GLP laboratory practices or a regulated environment
  • Ability to work collaboratively in a team-based laboratory environment
  • Desire to learn, gain and grow new skills in a fast-paced setting
  • Technical understanding of analytical control strategy and regulatory documentation experience
  • Experience leading or coordinating matrix teams
  • Experience with project management tools (Smartsheet, MS Project)
  • Familiarity with data trending and contract negotiations (MSAs, CDAs)
  • Familiarity with operating budgets and cost tracking

Responsibilities

  • Coordinate execution for external quality control testing including sample shipments between locations
  • Serve as single point of contact between PD and APS teams for studies and testing needs
  • Manage internal routine testing processes including scheduling, verification, and reporting
  • Create/manage data tracking systems for QC/CTL sites and internal data
  • Develop/manage inventory systems for instrumentation, reagents, and materials
  • Assist with method validation and transfer activities with internal and external partners
  • Assist with organization and coordination of MSAs/contracts
  • Support budgeting activities as needed
  • Communicate operations status updates clearly to leadership and teams
  • Maintain training and competency on internal analytical methods and provide lab-testing support
  • Participate in seminars, journal clubs, and continual professional development

Job description

Dispatch Biotherapeutics, Inc. is seeking a Senior Scientist to support Analytical Operations for our portfolio of product candidates, including viral vectors and CAR T cells. You will build and manage an efficient operational network, coordinate external testing with CDMOs, and ensure high-quality data generation and method transfer activities.

The role requires a Ph.D. with 5+ years or equivalent industry experience, strong GMP/GLP familiarity, and excellent collaboration across internal teams

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