Qualtiy Assurance Engineer

HyperLight is at the forefront of the commercialization of thin-film lithium niobate (TFLN) integrated photonics - a material and process technology that is enabling high-performance, scalable optical components across AI/datacom infrastructure, hyperscale computing, quantum computing, sensing, and beyond. Founded in 2018 and backed by leading venture capital, we’ve built a team and a platform focused on real-world mass deployment of TFLN photonics technology.

At the core of our work is the TFLN Chiplet™ platform — a modular, integrated architecture designed for scalability, manufacturability, and seamless integration into complex systems. It offers a rare combination of extraordinary performance and industrial readiness, enabling system developers across applications to deploy the technology fast and ready. We partner with our customers and suppliers from conceptualization, design, and prototyping phases, all the way through mass production to ensure smooth and rapid deployment of TFLN photonic technology.

We believe our platform is the key, in the golden age of integrated photonics, to empower humanity to the next level. We assembled a world class team covering engineering, business, and operations. We believe in the power of integrity, innovation, collaboration, and pragmatic solutions. Our diverse team thrives on challenges and is united by a shared commitment to excellence. We take pride in tackling complex challenges with curiosity, humility, and a deep sense of care for one another.

Our growing team is looking for a Quality Engineer to join our team in Cambridge, MA. In this role, you will ensure that incoming materials, in-process work, and finished products consistently meet defined quality standards. Your responsibilities will span IQC and OQC inspections, document control, change control evaluation, and internal auditing – all in support of a quality management system registered to ISO 9001, enabling the organization to deliver reliable, specification-conformant products while maintaining continuous improvement and regulatory readiness.

As part of your responsibilities, you will:

Inspection

Receive and sample-inspect incoming materials, components, and sub-assemblies against defined specifications (IQC)

Operate measurement equipment including calipers, microscopes, and fiber-alignment tools at the inspection workstation

Perform final acceptance inspection on finished products prior to shipment (OQC)

Verify test reports, certificates of conformance, and labeling completeness

Raise non-conformance reports (NCRs) and coordinate quarantine or return-to-vendor (RTV) actions

Log inspection data and maintain lot-traceability records

Document Control

Maintain and version-control SOPs, work instructions, inspection criteria, and engineering drawings On SharePoint and Notion

Ensure obsolete documents are withdrawn from production and correctly archived

Coordinate periodic document review cycles and manage document owner reminders

Review new or revised SOPs, test procedures, and inspection plans for technical accuracy and compliance

Provide QE sign-off within the document approval workflow (ECO / DCO routing)

Ensure approved documents are available at both sites prior to implementation

Auditing

Plan and execute internal process audits against ISO 9001 and applicable standards

Write audit reports documenting findings, observations, and opportunities for improvement (OFIs)

Track corrective action closure from prior audit findings

Conduct or support supplier quality audits and assess vendor quality systems

Serve as host and liaison during customer or third-party certification audits

Change Control

Evaluate engineering change requests (ECRs/ECOs) for quality impact on product, process, and documentation

Facilitate FMEA updates and risk assessments triggered by engineering changes

Determine re-validation or re-qualification requirements resulting from changes

Coordinate document updates, training, and material disposition in support of approved changes

Monitor change implementation on the production floor and verify effectiveness prior to closure

General Support Activities

Support and maintain the company Quality Management System (QMS) in accordance with ISO standards

Assist with planning and execution of supplier audits and supplier quality assessments

Drive corrective and preventive action (CAPA) processes including root cause analysis, corrective actions, and effectiveness verification

Collaborate with cross‑functional teams including design, product/test engineering, reliability, and operations to resolve quality issues

Assist/Work with external semiconductor manufacturing partners including wafer foundries and OSAT assembly/test suppliers to ensure product quality and process control

Support supplier quality management activities including supplier qualification, supplier corrective actions, and supplier performance monitoring

Support failure a…