Patient first
Every decision traces back to a person waiting for a therapy. It's the standard we hold each other to, on the floor and in the lab.
Careers
Work where the science reaches the patient.
At Solua, the batch on the floor is somebody's best hope. If you want your work to matter at that scale — and to learn at the leading edge of living medicines — there's a place for you here.
Why work here
A culture built around three commitments.
We're a science company that happens to manufacture — and a manufacturer that never loses sight of the science.
Rigor as craft
We take pride in the discipline of good science and good manufacturing. Quality isn't a department here — it's how we work.
Genuine partnership
We treat each other — and our clients — as collaborators. The best ideas win, regardless of title, and credit is shared.
Life at Solua
Invested in the people doing the work.
Hard science is demanding. We make sure the support around it is real.
- Comprehensive medical, dental and vision coverage
- Equity participation for every full-time employee
- Generous paid time off and recharge weeks
- Annual learning stipend and conference support
- Paid parental leave and family-care benefits
- Relocation support across our facility network
Open roles
Where we're hiring now.
Don't see your exact role? We're always glad to meet talented people — write to us at careers@soluatherapeutics.com.
Senior Process Development Scientist, Cell Therapy
Verdance Park, Cambridge, MA
Design and characterize robust, scalable autologous and allogeneic cell-therapy processes. You'll own development from feasibility through tech-transfer-ready, partnering closely with analytics and manufacturing.
ApplyGMP Manufacturing Associate II, Viral Vector
Solway Bioworks, Galway, Ireland
Execute closed-system viral-vector manufacturing in single-use GMP suites. You'll run upstream and downstream operations, complete electronic batch records, and uphold our quality system at the bench.
ApplyAnalytical Scientist, Potency & Bioassay
Verdance Park, Cambridge, MA
Develop and qualify mechanism-relevant potency and identity assays for cell, vector and EV programs. You'll build methods that survive validation and travel cleanly through technology transfer.
ApplyRegulatory Affairs Manager, CMC
Auterra Campus, Singapore
Author CMC sections and shape regulatory strategy for advanced-therapy programs. You'll be the bridge between our scientists and health authorities, turning data into defensible submissions across the Asia-Pacific region.
ApplyBring your best science here.
Tell us what you're great at. We'll tell you where it fits in the mission to make living medicines manufacturable.