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Light Labs

ZK-based on-chain state compression for Solana

Quality Control Lead

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAnn Arbor, MI, USA

About the Job

Requirements

  • Owned a quality subsystem end to end, such as CAPA, internal audit, document control, training, or method validation, in an accredited testing lab or regulated manufacturing environment, as part of a longer run in quality.
  • Supported an ISO/IEC 17025 accreditation assessment directly and have working knowledge of the standard.
  • Run out-of-specification and deviation investigations, including root cause analysis and CAPA closure.
  • Applied control chart methodology and quality control trending in practice.
  • Written investigations, standard operating procedures, and audit responses that held up under review.
  • Worked in laboratory information management system and quality management system software and understand the terminology.
  • Have a degree in chemistry, biology, engineering, or a related field.
  • Be ready to work on-site in Ann Arbor, Michigan, including regular time on the lab floor, personal protective equipment in lab areas, and occasional travel to Salt Lake City.
  • Explain the rationale for quality changes, bring technicians and scientists along, and step into the Quality Director's role when needed.

Responsibilities

  • Maintain the ISO/IEC 17025 quality management system, including the quality manual, standard operating procedure lifecycle, document and record control, and revision history.
  • Own change control for methods, instruments, software, and procedures, including impact assessments.
  • Run the internal audit program from scheduling through closure.
  • Prepare for and host accreditation assessments, and close findings with evidence.
  • Maintain consistent quality systems across the Ann Arbor and Salt Lake City laboratories.
  • Perform initial reviews of out-of-specification and out-of-trend results, decide whether results are fit to release, and escalate when they are not.
  • Lead nonconformance, deviation, and corrective and preventive action investigations from initiation through root cause analysis to effectiveness checks.
  • Investigate client complaints and quality inquiries and write responses.
  • Ensure laboratory information management system records and instrument raw data are attributable, legible, contemporaneous, original, and accurate.
  • Set control chart limits, review charts on a defined cadence, and act on shifts and trends.
  • Manage proficiency testing and interlaboratory comparisons and investigate unsatisfactory scores.
  • Support method validation and verification, including precision, accuracy, detection limits, and measurement uncertainty.
  • Maintain equipment qualification and calibration records, track stability studies, and run the Environmental Monitoring Program.
  • Report out-of-specification rates, corrective and preventive action aging, proficiency testing performance, and on-time closure into management review, and flag trends indicating process or equipment problems.
  • Qualify and monitor subcontracted and reference laboratories, review their results before they reach client reports, and evaluate critical suppliers and consumables that affect result quality.
  • Own analyst authorization, requalification, and documented evidence of analyst competency.
  • Work with the software team to build quality checks into the laboratory information management system and automation, and work with technicians and chemists to maintain consistent standards across workflows.
  • Track changes to ISO/IEC 17025, FDA, and USP requirements and translate them into practice.

Desired Qualifications

  • Dietary supplement, food, or consumer goods testing experience, including heavy metals, pesticides, microbiology, or nutritional analysis.
  • FDA current Good Manufacturing Practice (21 CFR 111 or 117), USP methods, and state or retailer requirements such as Proposition 65, California Assembly Bill 899, or Amazon requirements.
  • Experience supervising or mentoring quality or laboratory staff.
  • Quality work across more than one site or laboratory.
  • ASQ Certified Quality Auditor, Certified Quality Engineer, or Certified Manager of Quality/Organizational Excellence certification, or formal internal auditor training.
  • Experience validating software or automated data flows in a regulated environment.

About the Company

Light Labs

ZK-based on-chain state compression for Solana

Light Protocol lowers on-chain storage costs on Solana by using a ZK Compression framework that stores most account data off-chain while keeping a small Merkle root on-chain. Developers use an open-source protocol and SDKs; zero-knowledge proofs (Groth16 SNARKs) verify all state transitions, keeping data integrity intact. It stays on Solana’s Layer 1 rather than moving to a separate Layer 2, aiming to reduce rent and enable mass-market apps with full ecosystem compatibility. The goal is scalable, affordable, and privacy-conscious decentralized applications on Solana without sacrificing security or performance.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Not listed
Founded
2024

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