Research Technologist-cGMP Manufacturing

## Research Technologist-cGMP Manufacturing Apply locations:
Cancer Cell Center (CCC) time type:
Full time posted on:
Posted 2 Days Agojob requisition :
R-21017##
*
* Title:

** Research Technologist-cGMP Manufacturing
** Job Type:
** Regular##
** Company:
** Health Research, Inc. (HRI) Roswell Park Division##
** Department:
** Center for Immunotherapy##
** Time Type:
** Full time##
** Weekly

Hours:

** 40
* * FTE:
** 1##
** Shift:
** First Shift (United States of America)##
*
* Summary:

** About the Role    In this role, you’ll support important clinical and scientific research that helps move new discoveries forward. Working closely with experienced researchers and supervisors, you’ll assist with hands-on lab work and manufacturing activities that directly contribute to advancing cancer treatment and care.
This position also includes work in our cGMP clean room facility, where precision, consistency, and quality are essential. If you enjoy structured, detail-oriented work and want to be part of a team that brings research into real-world application, this is a great opportunity.  Pay Range: $52,979 - $67,185 annually, plus a comprehensive benefits package    What You’ll Do    Assist with laboratory experiments, procedures, and research activities  Support daily operations within a cGMP clean room manufacturing environment    Record and input clinical and research data into database systems  Help prepare and organize research findings, including initial observations for review  Perform routine maintenance and upkeep of laboratory equipment and machinery  Follow established protocols to ensure accuracy, safety, and compliance  Collaborate with team members to support ongoing research and production goals      

What You’ll Bring    An interest in scientific research, laboratory work, or manufacturing operations  Strong attention to detail and ability to follow precise protocols  Comfort working in a structured, regulated environment such as a clean room  Basic understanding of laboratory or clinical research practices (experience is a plus)  Good organizational and documentation skills  Ability to work both independently and as part of a team  A proactive mindset and willingness to learn new techniques and processes      Why You’ll Love Working Here    At Roswell Park Comprehensive Cancer Center, your work contributes to something bigger—helping bring new treatments and hope to patients.  

Here’s what you can expect:
Meaningful impact – Play a role in research and manufacturing that supports life-saving advancements  Hands-on experience – Build practical skills in both laboratory and regulated production environments  Collaborative culture – Work alongside dedicated scientists, clinicians, and support teams  Growth opportunities – Expand your knowledge in research, clinical operations, and cGMP processes  Comprehensive benefits – Support for your health, financial well-being, and work-life balance      This is a great opportunity for someone who enjoys hands-on work, thrives in a team setting, and wants to be part of advancing cutting-edge research into real-world treatments.##

*
* Qualifications:

** Required

Education and Experience    1. Master’s degree in a clinical or scientific discipline; or  2. Bachelor’s degree in a clinical or scientific discipline and the equivalent of one (1) year of full-time experience in a laboratory setting.

NOTE:

Required degrees must have been granted by an accredited college or university or one recognized by Roswell Park Comprehensive Cancer Center as following acceptable educational practices.

The preferred candidate will have:
* Hands-on experience in cell therapy such as CAR-T, or other adaptive cell transfer modalities process development, or manufacturing.
* Cell Therapy

Experience:

T-cell isolation, activation, transduction, expansion and Viral vector handling (lentivirus/retrovirus)
* Experience with cell selection/processing platforms like CliniMACS Prodigy and CliniMACS Plus
* Strong knowledge in Batch records, SOPs, Deviations & CAPAs, Change controls
* Working knowledge of cGMP standards, FDA/EU/ICH guidelines related to manufacturing of cell-based products is strongly preferred.
*…