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Adicet Bio, Inc is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for cancer and immunological disorders. We are advancing a pipeline of “off-the-shelf” gamma delta T cells, engineered with chimeric antigen receptors (CAR) and T cell receptor-like antibodies (TCRL). These are designed to enhance selective antigen targeting, facilitate innate and adaptive anti-tumor or other immune responses, and improve persistence for durable activity in patients. Our approach to activate, engineer, and manufacture allogeneic gamma delta T cell product candidates derived from the peripheral blood cells of unrelated donors allows us to generate new product candidates in a rapid and cost-efficient manner. For more information, please visit our website at http://www.adicetbio.com.

Sr. Research Associate, Quality Control

We are currently seeking an energetic and experienced individual with viral vector and/or cell therapy quality control background to join our Quality Control (QC) team. The successful candidate will contribute to the advancement of Adicet’s product pipeline by performing QC analytical method qualification, execute sample analysis and other assigned tasks. You will also be expected to independently organize, analyze and present results and conclusions.

The individual will work as part of the QC team in collaboration with Analytical Development, Process Development Groups, Research teams, and external collaborators, working collectively to meet project timelines.

Key Responsibilities

• Perform flow cytometry, ELISA, cellular cytotoxicity, qPCR, and other analytical assays to enable the characterization, release testing and stability monitoring of viral vector and cell therapy products and in-process samples.
• 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. Function as a subject matter expert in technical discussion, document review and investigation.
• Author and/or review analytical test results, technical and regulatory documents including but not limited to analytical study data summaries and reports, analytical method qualification protocols and reports, standard operating procedures (SOP).
• Perform data analysis and present results to the team.
• Work with QC team to maintain QC lab operation in GMP compliance.

Qualifications:

• BS or MS in biological sciences or a related field is required.
• 2 years of relevant experience in Pharmaceutical or Biotechnology industry.
• Hands on experience with PCR and qPCR is desired.
• Hands on experience in cell culture, cell-based assays and immunoassays is required.
• Experience in multi-parameter/multi-color flow cytometry is strongly preferred.
• Experience working in a regulated environment is preferred.
• Experience in writing SOPs is preferred.
• 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.

Benefits:

Adicet Bio offers both comprehensive benefits and Paid Time (PTO) plans for employees, which begin on the first day of employment, as well as the opportunity to work in a growing, dynamic environment.

Adicet Bio is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.