About this role
Role Overview
As a Quality & Compliance Engineering Expert, you will play a pivotal role in advancing frontier agent evaluations in quality engineering by developing long-horizon quality tasks. These tasks will be designed to reflect your existing work and will be accompanied by deterministic rubrics that assess agent performance against verifiable ground truth, ensuring that answers are checkable and free from subjective judgment.
Key Responsibilities- Develop scenarios related to Non-conformance and CAPA, including NCRs with required fields and CAPAs with documented root causes and containment actions.
- Prepare for audits by crafting responses aligned with specific ISO/FDA clauses, ensuring correct citations are included.
- Create verification and validation protocols, including inspection protocols and IQ/OQ/PQ, with clearly defined acceptance criteria and pass/fail outcomes.
- Engage in challenging tasks that require extended periods of focused work.
- Bachelor''s degree in Engineering.
- Minimum of 3 years of experience in quality engineering or compliance within a regulated industry such as medical devices, aerospace, automotive, or pharmaceuticals.
- Expertise in standards such as ISO 9001, ISO 13485, FDA QSR / 21 CFR 820, IATF 16949, AS9100, ISO 14971, and CAPA methodology.
- Proficient in reading and producing quality artifacts including NCRs, CAPAs, audit responses, and V&V protocols.
- Strong written communication skills, with the ability to articulate reasoning clearly and encode it into deterministic rubrics.
- ASQ CQE/CQA or equivalent certification is a plus.
This is a remote position with an hourly employment structure.
CompensationCompensation ranges from $75 to $100 per hour, depending on domain depth and prior experience. Strong contributors will have opportunities for promotion based on task quality and throughput.