Gene & Cell Therapy Scientist Job at Freyr Solutions (Client: Pharmaceutical Company)

Freyr Solutions (Client: Pharmaceutical Company) Boston, MA 02115

Gene & Cell Therapy Scientist:

The Biologics Discovery & Engineering department in Boston, MA is seeking a contractor to support developing chimeric antigen receptor (CAR) based cell therapies.

In this role, the successful candidate will contribute directly to the invention of novel gene and cell therapies. Responsibilities: • Perform PBMC isolation • Conduct cell culture to support engineering for primary T cells • Generate genetically engineered cells by lentiviral transduction • Support functional characterization of genetically engineered lymphocytes • Support lab operations • Record experimental design and results in electronic lab notebook, summarize findings and plan follow-up experiments with supervisor.

Requirements: • MS in a life science discipline with 5+years or BS/BA with 7+year post-graduate hands-on work experience in conducting lab-based research(academia/industry) or with PHD 2+ years of relevant experience. • Proficiency in cell culture and lentiviral transduction • Previous experience in immune based assay (Flow cytometry, MSD, etc) • Strong interpersonal, verbal, and written communication skills. Software: MS office(Power Point,EXCEL, word), FlowJo

Preferred Experience and Skills: • Familiarity with cell engineering via viral or CRISPR- based method is highly valued • Experience in high-throughput library design and screening, viral/non-viral transgene delivery, iPSC derived immune cells, and cell line engineering are desired.

Job Types: Full-time, Contract

Pay: $45.00 - $55.00 per hour

Schedule:

  • 8 hour shift
  • Monday to Friday

Ability to commute/relocate:

  • Boston, MA 02115: Reliably commute or planning to relocate before starting work (Required)

Experience:

  • cell culture: 2 years (Preferred)
  • lentiviral transduction: 2 years (Preferred)
  • lentiviral transduction (Flow cytometry, MSD, etc): 2 years (Preferred)
  • cell engineering via viral or CRISPR: 2 years (Preferred)

Work Location: One location




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