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Biomanufacturing Associate II

Elevatebio

Waltham, Massachusetts, United States (ElevateBio) permanent

Posted: February 24, 2026

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Quick Summary

This is a job summary for ElevateBio. The job involves supporting the manufacturing team at our BaseCamp facility, performing routine cGMP manufacturing of cell and gene therapy products.

Job Description

ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.

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.

Why Join ElevateBio?

ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.

We aim to be the dominant engine inside the world’s greatest scientific advancements harnessing human cells and genes to alter disease.

Our Mission:
To power the creation of life-transforming cell and gene therapies, at a speed the world deserves.

Our Vision:
We seek to be the world’s most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.

ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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