Research Technologist-cGMP Manufacturing

Research Technologist-cGMP Manufacturing

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

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

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

At Roswell Park Comprehensive Cancer Center, your work contributes to something bigger—helping bring new treatments and hope to patients.

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.

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.
• Solid foundation in aseptic technique and mammalian cell culture, with a track record of maintaining sterility and culture integrity in high-throughput or regulated settings.
• Strong communication skills, with the ability to convey scientific concepts clearly across cross-functional teams; collaborative, articulate, and committed to scientific excellence.
• Hands-on experience in cell therapy such as CAR-T, stem cell-based platforms, or other adaptive cell transfer modalities spanning research, process development, or manufacturing.
• Exceptional attention to detail, especially in good documentation practice, cleanliness, and organization critical qualities for maintaining reproducibility and regulatory compliance.