Research Technologist – Analytical Development and Quality Control; GMP

Position: Research Technologist – Analytical Development and Quality Control (GMP)
Research Technologist – Analytical Development and Quality Control (GMP) page is loaded## Research Technologist – Analytical Development and Quality Control (GMP) locations:
Cancer Cell Center (CCC) time type:
Full time posted on:
Posted Todayjob requisition :
R-20453##
*
* Title:

** Research Technologist – Analytical Development and Quality Control (GMP)
** 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:

** Join a mission-driven team at the forefront of cutting-edge cell and gene therapies. At Roswell Park’s state-of-the-art GMP Engineering & Cell Manufacturing (GEM) Facility, we are pioneering advanced immunotherapies like CAR-T with the goal of transforming patient care.
We are seeking a Research Technologist to play a key role in Analytical Development and Quality Control for the release testing of cell therapy products. This is a hands-on, lab-based position within a dynamic cGMP environment, ideally suited for individuals passionate about cellular therapeutics and high-impact translational research.

Key Responsibilities:

• Execute analytical development and QC release testing of cell and gene therapy products under cGMP conditions, including endotoxin, sterility, qPCR, dPCR and potency assays.  
• Draft, Review and maintain Standard Operating Procedure (SOPs), worksheets, forms, and QC release reports.  
• Set up, calibrate and maintain QC instruments, perform Preventative Maintenance, and/or conduction of IQ/OQ/PQ.  
• Ensure compliance with GMP/FDA guidelines and regulatory requirements for product release  
• Collaborate cross-functionally with Manufacturing Sciences, Process Development, Vector Development, and Quality Assurance teams to ensure seamless technology transfer, method suitability and qualification studies.  
• Contribute to continuous improvement initiatives to optimize processes and ensure readiness for clinical trial demands and regulatory audits.

What You’ll Bring :  
• A strong foundation in cell culture and aseptic technique, ideally in a cGMP or regulated environment.  
• A detail-oriented mindset with a commitment to quality and operational excellence.  
• Effective communication and teamwork skills to support cross-departmental projects.  
• Adaptability and drive to work in a fast-paced, evolving field at the intersection of science and medicine.

• Be part of a nationally recognized cancer center with a legacy of innovation and patient-centered care.  
• Access to world-class facilities, resources, and training to support your professional growth.  
• The opportunity to directly contribute to life-saving therapies that make a difference in patients’ lives.
Behavioral & Professional

Competencies:

• Strong interpersonal skills and the ability to communicate clearly across functions and teams.  
• Highly organized with the ability to manage multiple tasks and meet tight deadlines.  
• Excellent verbal and written communication skills.  
• Resourceful and solutions-focused mindset with a strong sense of ownership.  
• Adaptable and resilient in a fast-paced, mission-critical setting.
The starting annual compensation for this position is $50,456 and this includes a full comprehensive benefits package.##
*
* 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 school, college or university or one recognized by Roswell Park Comprehensive Cancer Center as following acceptable educational practices.
* Extensive experience in Analytical Development or Quality Control settings
* Demonstrated proficiency in cellular and molecular assays, such as flow cytometry, cytotoxicity, qPCR, dPCR, ELISA, and a strong analytical mindset and troubleshooting capabilities.
* Working knowledge of cGMP standards, FDA/EU/ICH guidelines related to…