About The Role

FISBA North America/ Senior Quality Engineer / Saco, Maine

FISBA is seeking a Senior Quality Engineer, to be based in their Saco, Maine facility. FISBA is a global company dedicated to shaping light through excellence in optical design, system engineering, high precision volume production and advanced optical coating. In the broad field of photonics, FISBA focuses on solutions for Life Sciences, Advanced Manufacturing and Aerospace and Defense – always with the mission of empowering customers to exceed their goals.

Job Summary

This hands-on role owns the incoming and outgoing inspection processes, performs quality inspections as needed, manages inspection equipment, and supports effective execution of inspection activities. The Senior Quality Engineer also works closely with process owners to maintain and improve the Quality Management System (QMS), implements processes in the CAQ Process module as needed, and supports engineering and production process development and production transfers.

What We Offer

Generous paid vacation and sick time
8 paid holidays and 2 floating
Paid parental leave
Medical, dental, vision
HSA with employer contribution
401k with employer match
Annual pay in the range of $95,000 - $120,000

Qualifications

Bachelor’s degree in Quality Engineering, Manufacturing Engineering, Mechanical Engineering, or a related technical field; equivalent relevant experience may be considered.
Five or more years of quality engineering or manufacturing quality experience, preferably in a medical device manufacturing environment.
Hands-on experience with incoming, in-process, final, and outgoing inspection processes.
Working knowledge of ISO 13485 quality systems and medical device manufacturing requirements.
Experience using electronic Quality Management Systems (eQMS), SAP, and computer-aided quality systems; CAQ experience is preferred.
Experience managing inspection and measurement equipment and supporting calibration and maintenance controls.
Experience with engineering and production process development, process validation, and production transfers.
Ability to interpret drawings, specifications, acceptance criteria, inspection plans, and test results.
Demonstrated ability to work hands-on with Production, Engineering, Supply Chain, and other process owners to resolve quality issues and improve processes.
Strong written and verbal communication skills, with the ability to train personnel, lead working sessions, and collaborate effectively across the organization.

Responsibilities and Scope

Own and continuously improve the incoming and outgoing inspection processes, including final-test review and product-release inspection activities.
Perform incoming, in-process, final-test, and outgoing quality inspections as workload and business needs require.
Manage quality inspection equipment, including equipment readiness, calibration status, maintenance coordination, and appropriate use.
Supervise and support execution of the inspection process to ensure requirements, records, and acceptance criteria are consistently applied.
Partner directly with process owners to update, document, implement, and improve quality processes within the QMS.
Implement and maintain processes in the CAQ Process module as needed.
Support engineering and production process development, validation, and transfer into manufacturing.
Implement process controls, inspection methods, test methods, and validation protocols for medical device manufacturing.
Support nonconformance, CAPA, risk management, change management, supplier quality, internal audit, and continuous-improvement activities.
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