[Hiring] Scientific Product Specialist @Alchemi

Role Description

We're hiring Scientific Product Specialists to be the scientists in the room. You'll work hands-on with customer teams to understand exactly how a study gets run and reported today, configure Alchemi to fit it, and make sure what our agents produce would stand up to an FDA reviewer.

You'll sit between customers, our engineers and our product team. When something in the output isn't right, you're the one who spots it, explains why, and makes sure it gets fixed properly. What you see in the field will shape what we build next.

What you'll do

• Lead the scientific side of customer deployments, from kickoff to go-live.
• Map customer workflows, templates, SOPs and data, and configure our agents and blueprints to match.
• Review agent output for scientific and regulatory accuracy, and turn what you find into clear feedback for engineering.
• Train customer scientists and become their trusted contact at Alchemi.
• Bring patterns from across customers back into the product roadmap.

Qualifications

• An advanced degree (MS or PhD) in a relevant science, or equivalent hands-on experience.
• Several years in pharma, biotech or a CRO, ideally writing or reviewing regulated study reports.
• Working knowledge of GxP and what makes a document defensible to QA and regulators.
• Comfort in front of customers and willingness to travel.
• Excitement about AI changing how scientific work gets done, and the rigor to hold it to a high standard.

Requirements

• Direct experience in bioanalysis, toxicology, CMC or regulatory submissions.
• Experience at a startup or in a customer-facing scientific role.

Company Description

It takes more than a decade and over $2 billion to bring a new drug to market. A lot of that time is spent writing, reviewing, and defending documentation in regulated environments where mistakes are expensive and speed is hard to come by.

Alchemi builds AI agents purpose-built for that work. Our platform drafts regulatory documents from a team's own templates, runs QC and QA review against the guidelines and SOPs that actually govern a study, and does it inside a single-tenant, GxP-compliant environment that never trains on customer data. We're already working with three of the top five pharma companies, and our agents are in use across non-clinical, clinical, bioanalysis, CMC, regulatory submissions, and safety.