Sr. Research Associate
Quality Control
Confirmed live in the last 24 hours
Adicet Bio, Inc

51-200 employees

Develops allogeneic gamma-delta T cell therapies for cancer.
Company Overview
Adicet Bio, Inc. stands out as a leader in the cell therapy space, focusing on the development of allogeneic gamma-delta T cell therapies, a unique approach that offers multiple ways to target and kill cancer cells. The company's "off-the-shelf" model, using cells from unrelated donors, allows for rapid, cost-effective scaling of medicine production, ensuring availability when needed. With a dedicated team working towards defeating cancer, Adicet fosters a culture of purpose, innovation, and patient-centricity, making it an ideal workplace for those passionate about making a significant impact in the biotechnology industry.
Biotechnology

Company Stage

N/A

Total Funding

$243.6M

Founded

2014

Headquarters

Redwood City, California

Growth & Insights
Headcount

6 month growth

-3%

1 year growth

20%

2 year growth

73%
Locations
San Carlos, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
Data Analysis
CategoriesNew
Lab & Research
Life Sciences
Requirements
  • BS or MS in biological sciences or a related field
  • 2+ years of relevant experience in Pharmaceutical or Biotechnology industry
  • Hands on experience with PCR and qPCR
  • Hands on experience in cell culture, cell-based assays and immunoassays
  • Experience in multi-parameter/multi-color flow cytometry
  • Experience working in a regulated environment
  • Experience in writing SOPs
  • Ability to work independently, multitask and meet deadlines in a fast-paced environment
  • Highly motivated, organized and detail oriented
  • Excellent computer, verbal and written communication skills
Responsibilities
  • Perform flow cytometry, ELISA, cellular cytotoxicity, qPCR, and other analytical assays
  • Support analytical method development, qualification, and technical transfer to Contract Testing Laboratories (CTL) and Contract Development Manufacturing Organizations (CDMO)
  • Support management of CTL and CDMO analytical activities
  • Author and/or review analytical test results, technical and regulatory documents
  • Perform data analysis and present results to the team
  • Work with QC team to maintain QC lab operation in GMP compliance