The Role:

ElevateBio is seeking a proactive and driven professional to join our Manufacturing team at our BaseCamp facility. In this role, you will support and perform routine cGMP manufacturing of a diverse portfolio of cell and gene therapy products. We’re looking for someone who is a motivated self‑starter with a passion for innovative science and a desire to contribute to a manufacturing organization unmatched in its capabilities and expertise. The ideal candidate is enthusiastic about learning new technologies, thrives in collaborative, cross‑functional environments, and is committed to upholding the highest standards of safety and quality.

Here’s What You’ll Do:

• Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, expansion, harvest, cryopreservation and final product visual inspection.
• Perform manufacturing/operations activities including but not limited to reviewing SOPs /batch records, material ordering/management.
• Participate in and, if applicable, provide training to team on set-up and use of equipment, process and material flows, as assigned.
• Commitment to the highest safety and quality standards in service of our colleagues and patients.
• Ensure clean rooms and equipment are maintained in an organized and ready state.
• Work effectively with cross functional teams comprised of process development, facilities & engineering, MSAT, quality control, quality assurance, to ensure right-first-time technology transfer and routine cGMP production.
• Work closing with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, Change Controls.
• Execute and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.
• Proactively identify opportunities for improvements in process, safety, quality, and cost

Requirements:

• Bachelor’s degree in biological science(s) field or related engineering with:
• 2-4 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
• Experience with cGMP manufacturing and/or process development for CAR T, TCR, TIL, cellular therapies, mRNA.
• Project leadership experience is a plus.
• Strong understanding of primary cell culture and experience with equipment including but not limited to CliniMACS Plus, CliniMACS Prodigy, LOVO, Incubators, Centrifuges, CRF, and G-Rex system.
• Outstanding written and verbal communication skills
• Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.
• Demonstrated proficiency in aseptic technique and/or processing.
• Ability to function in dynamic environment and balance multiple priorities simultaneously.

Work Schedule:

• 8-hour day shifts, Monday through Friday.
• Must be available to work overtime on weekdays, weekends and holidays as needed.

Physical Requirements:

• Will frequently stand, walk, bend, stretch for extended periods.
• Routinely carry up to 25 pounds and up to 50 pounds.
• Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.
• Routine repetitive use of arms/wrist/hands.
• Ability to work nights, weekends, holidays as needed to support business needs

The budgeted range for this position is $38-$52/hr. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.