Home › Companies › ElevateBio › Biomanufacturing Associate II (Contract)
Biomanufacturing Associate II (Contract)
ElevateBio · Waltham, Massachusetts, United States · Active · Greenhouse
Job facts
| Field | Value |
|---|---|
| Company | ElevateBio |
| Title | Biomanufacturing Associate II (Contract) |
| Normalized title | - |
| Department / team | Manufacturing |
| Location | Waltham, MA, United States |
| Work model | - |
| Employment type | Contingent Worker |
| Salary | - |
| Status | active |
| ATS provider | Greenhouse |
| Posted / first seen | 2026-06-02 / 2026-06-03 |
| Changed / last seen | 2026-06-03 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from ElevateBio. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Greenhouse. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Waltham. | Open |
| Department jobs | Active postings in Manufacturing . | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | ElevateBio |
| Source | 65f4d397-8a87-4475-b044-9867238dbeb3 |
| ATS provider | Greenhouse |
Description
ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.
The Role:
ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.
Here’s What You’ll Do:
Perform and lead routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.
Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.
Provide training to team on set-up and use of equipment, process and material flows, as assigned.
Ensure clean rooms are maintained in an organized and ready state.
Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.
Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.
Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.
Work closing with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.
Commitment to the highest safety and quality standards in service of our colleagues and patients.
Generate 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 at least 2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.
Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.
Understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system is preferred.
Outstanding communication skills (verbal and written).
Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word
Demonstrate proficiency in aseptic technique and/or processing.
Ability to function in dynamic environment and balance multiple priorities simultaneously.
Work Schedule:
Rotating 7 Day 12-hour shifts. (7am-7pm)
Must be available to work overtime on weekdays, weekends and holidays as needed.
Physical Requirements:
Employee 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/hour - $52/hour. 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.
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.
Full job record
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| Org ID | 740be8c1-c887-4446-8d84-84a038d00038 |
| Source ID | 65f4d397-8a87-4475-b044-9867238dbeb3 |
| Board ID | 65f4d397-8a87-4475-b044-9867238dbeb3 |
| Provider | greenhouse |
| Provider Job Key | 6010448004 |
| Title | Biomanufacturing Associate II (Contract) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Waltham, Massachusetts, United States |
| Department | Manufacturing |
| Team | — |
| Employment Type | Contingent Worker |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MA |
| City | Waltham |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://elevate.bio/about/jobs/6010448004?gh_jid=6010448004 |
| Apply URL | https://elevate.bio/about/jobs/6010448004?gh_jid=6010448004 |
| First Seen At | 2026-06-03 10:48:06Z |
| Last Seen At | 2026-06-06 20:38:52Z |
| Last Checked At | 2026-06-06 20:38:52Z |
| Last Changed At | 2026-06-03 10:48:06Z |
| Inactive At | — |
| Source Posted At | 2026-06-02 15:31:59Z |
| Source Updated At | 2026-06-02 15:31:59Z |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=greenhouse/board=elevatebio/date=2026-06-06/2026-06-06T20-38-51-946Z-f3d26930708fd4d7faf366984c85c4e41b7a6e5385e37df01c856a432b87df02.json |
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