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Applied AI · Agents & Evals

Iver
Olsen

AI for engineering teams whose data is scarce, expensive, and regulated.

I spent fifteen years running materials labs and quality systems in medical devices — a world where one data point can cost hundreds of dollars and take ten weeks to get, a label can't be trusted until the measurement system is, and nothing ships until validation proves it works. Now I build AI systems held to that same standard: production RAG and agent systems with eval harnesses, acceptance criteria, and audit trails. There's a live system below and writeups on how it was built. I build for engineers and scientists because I've been both.

$500M
Portfolio Supported
85%
First-Pass Yield (from 11%)
$100M+
YoY Shipment Lift
500+
Lab Hours Saved / Year
Scroll
01

About

Iver Olsen

I see the gap before it's a problem

I started as a lab tech, running tensile tests and prepping metallographic samples, learning how materials behave before I ever managed anyone. Fifteen years later, I lead the materials and clinical engineering function for a $500M global operation. The technical foundation matters, but what stuck with me was everything around it: what it's like to be the person doing the careful, detailed work, what gets glossed over by the people relying on it, and how technical expertise turns into results the rest of the business can use. Those lessons shape how I lead now.

The pattern across all of it is the same: I see the gap, whether it's a missing lab, no quality system, no process, or no data, and I figure out how to stand it up, prove it works, and make it stick. Sometimes that means pointing the gap out to people who haven't noticed it yet. It's meant building an ISO 17025 quality system from scratch, turning around a plating line that was scrapping nearly nine parts in ten, standing up a BSL-2 microbiology program, and writing the EU MDR strategy for a $140M device portfolio. Lately the gap has been software: my teams were losing days to manual document searches and report writing, so I learned to build the AI tools that give that time back, with a bias toward systems that stay traceable and auditable instead of just demoing well.

The technical work is only half of what I do. The other half is building the team that carries it further than I could alone: engineers and scientists who trust each other, who stay, and who become the people their colleagues call when something breaks.

02

Selected Work

Applied AI · Live in production

Materials Science Literature RAG

A production RAG and agent system over materials-science corpora. Hybrid retrieval, a 95-case eval harness, and an agent that verifies its own citations against the sources, built solo and deployed live for around $12–20/month. The live app is invite-only; the full case study is public.

Hybrid BM25 + dense + RRF 95 labeled eval cases 13 ADRs · CI-gated ~$12–20/mo
03

Start Here

If you want to understand how I build AI for regulated, physical-world work, start with these. The first maps Lean Six Sigma onto machine learning; the others cover where AI actually pays off, and how I debug a retrieval system with evals.

04

Areas of Practice

The AI systems I build for engineering and quality teams, grounded in the fifteen years of materials and quality work they're built to serve.

Applied AI · Agents & Evals
Production RAG and agent systems for engineering and quality teams, built and deployed, not prototyped. That includes a live, public materials-science RAG with a 95-case retrieval eval harness, plus a certification pipeline and automated lab reporting running in production. I work deterministic-first: LLMs handle the genuinely ambiguous parts while evaluation and audit logic stay rule-based and traceable.
PythonRAGAgents & Tool UseEvalspgvectorFastAPI
Materials & Failure Analysis
Materials selection, characterization, and structured root-cause analysis across medical device, energy, and precision manufacturing. I start with the process, not the symptom, and drive to root cause before anyone jumps to a fix.
Failure AnalysisSEM/EDSMaterials SelectionRoot CauseDMAICXRF
Quality Systems & Regulatory
Design, implementation, and remediation of ISO 13485 and ISO 17025 quality systems, EU MDR and FDA 21 CFR Part 820 strategy, and IQ/OQ/PQ validation for Class I, II, and III devices, from scratch through accreditation and audits.
ISO 13485ISO 17025EU MDRFDA 21 CFR 820IQ/OQ/PQTechnical Files
Process & Lab Strategy
DMAIC-driven turnarounds for high-scrap manufacturing lines, laboratory insourcing strategy, KPI framework development, and Python analytics. I build lab programs from the ground up and the metrics to prove they work.
DMAICSPCLab InsourcingKPI DesignPythonProcess Mapping