Build the Future of Drug Safety

Join a team of scientists and engineers transforming how the pharmaceutical industry makes benefit-risk decisions.

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ArcaScience is building the analytical foundation for better drug safety decisions. Every feature we ship serves one mission: helping pharmaceutical companies make benefit-risk assessments that are faster, more rigorous, and more transparent. If you want your work to directly improve outcomes for millions of patients, you belong here.

What You'll Find Here

Meaningful Impact

Your work directly improves drug safety decisions affecting millions of patients. Every analysis, every model, every regulatory output contributes to safer medicines and better-informed benefit-risk assessments.

Scientific Rigor

Work alongside PhDs in pharmacoepidemiology, biostatistics, and regulatory science. We never compromise on methodological integrity. Our team includes former FDA reviewers, EMA consultants, and published researchers.

Technical Challenge

Process 100B+ data points with cutting-edge AI/ML infrastructure. Build domain-specific models for signal detection, causal inference, and comparative effectiveness. Scale systems that pharmaceutical giants depend on daily.

Global Team

15+ nationalities across Paris and Sunnyvale offices. Diverse perspectives from biotech, consulting, academia, and regulatory agencies. Collaborative culture where the best ideas win, regardless of seniority.

60+

Team members

40%

Scientists

40%

Engineers

15+

Nationalities

2

Global offices

Explore Our Teams

Engineering

Build the infrastructure processing 100B+ data points. Python, Rust, PostgreSQL, Kubernetes. ML pipelines, distributed systems, regulatory-grade validation.

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Science

Drive pharmacoepidemiology research and regulatory science. Signal detection methodology, BRAT framework implementation, AI model validation, regulatory submission support.

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Operations & Commercial

Scale ArcaScience's impact across the pharmaceutical industry. Client success, commercial strategy, partnerships, compliance, and operations roles supporting global growth.

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Join Our Team

Engineering Paris Full-time

Senior Backend Engineer

Build distributed systems processing 100B+ pharmacovigilance data points. Python, Rust, PostgreSQL, Kubernetes. Experience with ML pipelines and regulatory validation requirements.

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Engineering Sunnyvale Full-time

ML Research Scientist

Develop domain-specific AI models for signal detection, causal inference, and comparative effectiveness. PhD in ML/Statistics preferred. Experience with healthcare or pharmacovigilance data a plus.

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Science Paris / Remote Full-time

Senior Pharmacoepidemiologist

Lead benefit-risk methodology development and regulatory science strategy. PhD in pharmacoepidemiology or related field. 5+ years post-doc experience. Publications in regulatory science preferred.

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Science Sunnyvale Full-time

Regulatory Science Consultant

Support pharmaceutical clients through regulatory submission preparation. Experience with FDA, EMA, or PMDA submissions. PharmD or PhD with regulatory affairs background. Travel required (25%).

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Commercial Paris Full-time

Client Success Manager

Own pharmaceutical client relationships and drive platform adoption. Scientific background (PharmD/MSc/PhD) required. 3+ years in client-facing role at SaaS, biotech, or CRO preferred.

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Operations Sunnyvale Full-time

Compliance & QA Lead

Ensure FDA 21 CFR Part 11, GDPR, and ISO 27001 compliance across the platform. Experience with pharmaceutical software validation, audit management, and regulatory inspections.

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Don't See Your Role?

We're always looking for exceptional talent across all disciplines. Send us your CV and tell us how you'd contribute to ArcaScience's mission.

Send Us Your CV

Where We Work

[Photo: Paris Office Open Workspace]

Our Paris office near Gare de Lyon — collaborative workspace designed for cross-functional teams.

[Photo: Team Offsite Event]

Quarterly team offsites bring our Paris and Sunnyvale teams together for strategy, workshops, and team building.

[Photo: Conference Presentation]

Presenting at ICPE, DIA, and regulatory science conferences — our team stays at the forefront of pharmacoepidemiology research.

[Photo: Cross-Functional Collaboration]

Engineers, scientists, and commercial teams work side-by-side — the best solutions emerge when diverse perspectives converge.

What Guides Us

Scientific Integrity

We never compromise on methodological rigor. Every model, every analysis, every regulatory output is built on defensible scientific foundations. Our reputation depends on the quality of our work.

Patient Impact

Every feature we build serves the mission of safer medicines. Benefit-risk decisions affect millions of patients. That responsibility drives every technical choice, every priority, every deadline.

Collaborative Excellence

The best work happens when diverse perspectives converge. Engineers challenge scientists. Scientists challenge engineers. Junior team members ask the hard questions. Hierarchy never silences the best idea.

Ready to Make an Impact?

Join a team building the analytical foundation for better drug safety decisions.

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