Principal Engineer I/II, MSAT / Viral Vector Downstream
Listed on 2026-08-22
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Engineering
Validation Engineer, Manufacturing Engineer, Process Engineer, Quality Engineering
Job Title: Principal Engineer I/II, MSAT / Viral Vector Downstream
Department: External CMC Operations
Reports to: VP of External CMC Operations
Location: Onsite 5 days per week at our Berkeley, CA office
Employment Type: Full-time
FLSA Status: Exempt
Bonus/Equity: Eligible
About Azalea
Azalea Therapeutics is enabling precision genome engineering directly inside the body, with an initial focus on creating cancer immunotherapies in vivo. Azalea is pioneering a new way to turn a person’s own T cells into a powerful cancer therapy — directly inside the body. Instead of removing cells and manipulating them in a lab, we use precision genome editing tools to engineer T cells where they already live.
At the center of our approach are Enveloped Delivery Vehicles, or EDVs. As highly selective couriers, EDVs are designed to specifically locate T cells within the patient and deliver our genome engineering cargo. Once inside the cell, the anti-cancer agent is inserted into a precise site in the genome, ensuring safe and potent modifications to fortify the T cells against cancers.
Why This Matters
- We aim to make cell therapy faster and more accessible by avoiding complex manufacturing outside the body.
- Our platform is designed for precision, so the right cells are safely programmed to effectively fight cancer.
- This technology has the potential to treat a wide range of cancers with a streamlined, scalable process.
Our goal is simple: develop next-generation delivery technologies to bring genetic engineering and cell therapies to more patients.
How We Work
Azalea is building ambitious science in a fast-moving environment. The people who thrive here are accountable, adaptable, rigorous, humble, and direct. Across roles and functions, we look for team members who demonstrate the following:
The Opportunity
Azalea is seeking a Principal Engineer I/II, Manufacturing Science and Technology (MSAT) - Viral Vector Downstream to serve as the senior technical lead for downstream viral vector technology transfer, and manufacturing readiness. Reporting to the VP of External CMC Operations, the immediate focus for this role will be advancing the EDV and AAV manufacturing capabilities required to move pipeline programs toward first-in-human readiness, including pilot runs, engineering runs, and initiation of GMP manufacturing.
This is a senior individual-contributor role aligned with Azalea’s Principal Scientist I/II levels. The Principal Engineer will be accountable for the technical direction of a major manufacturing area, not only the execution of assigned activities. This person will work closely with the internal process development teams to define priorities, connect downstream process decisions to program and company goals, provide technical leadership across external manufacturing partners, mentor other contributors, and influence cross-functional decisions with limited oversight.
The ideal candidate is a hands-on downstream process expert who can move between detailed data analysis and broader CMC strategy. This person should be comfortable leading through influence in a lean, externally networked organization, making clear recommendations with incomplete information, and balancing speed, quality, manufacturability, regulatory expectations, and patient-focused progress. They will be responsible for managing the technology transfer of our EDV and AAV manufacturing processes to our external manufacturing partners for the current and future programs.
This is a full-time onsite position at our Headquarters in Berkeley, CA. The incumbent will travel and be onsite at the CDMO during manufacturing.
Key Responsibilities
- Define and lead the external downstream process strategy for Azalea’s viral vector programs, with an immediate focus on EDV and AAV manufacturing for Program 1.
- In collaboration with the PD team, assist with downstream process development, optimization, scale-up, and manufacturing readiness activities across clarification, filtration, chromatography, ultrafiltration/diafiltration, formulation interfaces, sterile filtration, hold-time strategy, and other relevant unit operations.
- Establish phase-appropriate process…
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