Quality Manager

Quality Manager LIGHTERA has one of the longest and most respectable corporate lineages in American business, which goes back to Alexander Graham Bell and the invention of the telephone more than a century ago. We have a proven track record of being first in the industry with application specific fibers, optical connectors, ribbon cables, erbium doped fibers, Raman fiber lasers, fiber gratings and more. Our mission is to provide leading optical innovations and solutions by designing, manufacturing and supplying the best optical fibers, fiber cable and components and devices for our customers, with exceptional service that creates value for our shareholders, customers and employees. To do so, we must continue shaping the future of communications by applying the best minds to the challenges our customers will continually face. We currently seek a Quality Manager to join our division located in Avon, CT, and help support our continued business growth. This position is a hands‑on leader responsible for the development, maintenance, and continual improvement of our integrated Quality Management System (QMS) to meet and sustain ISO 13485 and AS9100 certifications. This role drives product and process quality across a high‑mix, high‑complexity manufacturing environment serving regulated markets. The Quality Manager partners closely with Operations, Engineering, Supply Chain, and Program Management to ensure compliance, mitigate risk, improve yield, and elevate customer satisfaction. Essential duties and responsibilities include, but are not limited to: Quality Management System (QMS) As the QMS Management Representative, own the QMS to ISO 13485 and AS9100 requirements, ensuring alignment across procedures, records, and metrics. Lead Management Reviews, Quality planning, KPI alignment, and continuous improvement roadmaps. Ensure robust Document Control and Change Control (ECO/ECN) processes, including review/approval workflows and training effectiveness. Compliance, Audits & Regulatory Lead or support third‑party certification audits, customer audits, and regulatory inspections; manage audit schedules and responses Maintain compliance with FDA 21 CFR 820 (as applicable), AS9100, and customer‑specific quality clauses. Oversee CAPA, nonconformance (NCR), and complaint handling; ensure timely, effective root cause and verified closure. New Product Introduction (NPI) & Advanced Quality Integrate quality into the NPI lifecycle: phase‑gate reviews, risk management, PFMEA/DFMEA, control plans, validation protocols (IQ/OQ/PQ), and special characteristics management. Establish First Article Inspection (FAI) and PPAP/APQP where required for aerospace programs. Define and deploy receiving/in‑process/final inspection strategies tailored to high product mix with variable routings and cycle times. Manufacturing Quality & Continuous Improvement Champion Statistical Process Control (SPC), MSA/Gage R&R, and data‑driven problem solving (8D, 5‑Why, Fishbone, DOE). Drive process capability (Cp/Cpk), yield improvement, scrap/rework reduction, and robust process validation/verification. Lead MRB and material disposition; ensure effective containment, root cause, and systemic corrective actions. Implement standardized work, error‑proofing (poka‑yoke), and digital quality workflows where practical. Supplier Quality & Incoming Controls Build and manage the Supplier Quality Management system: qualification, risk‑based audits, scorecards, corrective action, and development plans. Define incoming inspection sampling plans (AQL, risk‑based), special process controls, and calibration integrity. Customer Quality & Program Support Serve as the voice of quality to customers: manage escape investigations, RMAs, complaints, and customer scorecards; drive proactive quality plans per contract. Support program launches and transitions, ensuring deliverables (FAI/PPAP, FAIRs, CoC/CoA, DMR updates) are right‑first‑time. Data, Systems & Tools Own quality data analytics and leading/lagging indicators; publish actionable insights for operations. Administer or partner on QMS/ERP/PLM/MES platforms, including electronic records/signatures. Oversee metrology and calibration systems; ensure gage lifecycle management and suitability for tolerance stacks common in high‑complex assemblies. Leadership & Culture Develop a high‑performing quality team: recruiting, coaching, training, succession planning. Build a quality‑first culture that balances compliance, speed, and customer focus; influence cross‑functional leaders and production teams. Promote EHS practices and safe qualitycorrect risks promptly and model safe behaviors. Key qualifications include: Bachelor's degree in Engineering, Quality, or related technical field. 8+ years of progressive quality experience, including 3+ years in a leadership role within high‑mix manufacturing. Demonstrated ownership of ISO 13485 and/or AS9100 certified QMS; audit leadership experience (internal/third‑party/customer). Hands‑on expertise with CAPA, risk management, FAI (AS9102), validation (IQ/OQ/PQ), and SPC/MSA. Proficiency with 8D, root‑cause analysis tools, and data‑driven decision‑making. Knowledge of blueprint reading, GD&T, complex assemblies, and tolerance analysis. Excellent communication skills and experience collaborating with customers and executive leadership. Preferred qualifications: Advanced degree or certifications: ASQ CQE/CQA/CMQ/OE, Lead Auditor (ISO 13485 or AS9100), Six Sigma Green/Black Belt. Experience in medical device and aerospace/defense environments simultaneously (mixed compliance). Familiarity with ITAR/EAR export controls. Experience implementing or migrating eQMS or MES, including Part 11‑compliant workflows. Working knowledge of sterilization or biocompatibility processes Working at LIGHTERA means having the opportunity to realize ideas, experience innovation and discover new solutions for the future. In addition to our dynamic work environment, we offer the following for our employees: Competitive salaries and generous benefits programs, including health, dental, vision and well‑being. Company‑sponsored 401(k) plan with a generous match and no vesting period. Tuition assistance, on‑the­job training and opportunities for growth and advancement. We promote from within. Generous Paid Time Off (PTO) program and paid holidays. Employees are expected to serve as role models for safe work practices and behaviors. This includes following established health and safety policies and procedures, maintaining a clean, organized work area, wearing, and properly storing all personal protective equipment (PPE), and actively engaging as a safety conscious worker with personal safety and wellness as a priority. If you'd like to be part of an energetic, world leader in optic fiber solutions, please apply through our Career portal at Note: Visa sponsorship not available. Applicants must be legally authorized to work in the United States now and in the future. The company does not provide visa sponsorship or any immigration support (including STEM OPT training plan) for this position. About Lightera Lightera is a global leader in optical fiber and connectivity solutions, delivering innovative technologies that drive communication networks, data centers, and specialty photonics applications. With a deep legacy of expertise in optical science, we provide high‑performance solutions that enable faster, more reliable, and more sustainable connections for businesses, communities, and industries worldwide. Headquartered in Norcross, Georgia, U.S.A., Lightera operates with a global footprint, serving customers across telecommunications, enterprise, industrial, generative AI, data centers, 5G/6G, utilities, medical, aerospace, defense, and sensing markets. Lightera is part of Furukawa Electric Group, a multi-billion‑dollar leader in optical communications. Lightera is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or status #J-18808-Ljbffr