Quality Engineer III

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.Objectives:The Senior Quality Engineer serves as a key Quality Assurance representative for contact lens manufacturing operations at the Rochester, NY facility. This role is accountable for ensuring compliance with applicable Quality Management System (QMS) requirements, including ISO 13485 and FDA 21 CFR Part 820, while driving continuous improvement in product and process quality.The position provides technical leadership across the product lifecycle, including design transfer, process validation, manufacturing, and postmarket quality activities, ensuring alignment with Bausch + Lomb global standards and regulatory expectations.The Senior Quality Engineer partners cross-functionally to implement risk based decision-making, support new product introductions, and lead quality improvement initiatives to enhance product performance, compliance, and operational efficiency.Key Activities/Responsibilities:Ensure compliance with qms requirements, including:Nonconformance (nc) management and capa systemsChange control and validation activitiesDocument review and approval (dhrs, sops, specifications)Provide quality oversight for:Contact lens product lifecycleProcess validation (sat/fat/iq/oq/pq/pv)Statistical sampling plans and data analysisDesign transfer activities in accordance with design control requirementsDrive root cause investigations using structured methodologies:Pdca, 5y, dmaic, 8d, fishbone, etc.Ensure timely and effective containment, correction, and preventionPerform data analysis and trending to:Identify emerging risks and quality signalsSupport decision-making through statistical toolsLead risk management activities aligned with iso 14971, including:Pfmea development and maintenanceRisk assessment, mitigation, and verificationAct as a quality lead for continuous improvement initiatives:Reduce scrap, defects, and cost of poor quality (copq)Improve manufacturing capability and process robustnessEnsure audit readiness and participate in:Internal auditsExternal regulatory inspections (e.g., fda, notified bodies)Collaborate with cross-functional teams (manufacturing, engineering, R&D, supply chain) to:Resolve quality issuesSupport product lifecycle activitiesEnsure alignment with design and regulatory requirementsMentor junior engineers, quality technicians and provide technical guidance to operations personnel and peersScope:The Senior Quality Engineer operates with a high level of independence and technical authority, influencing key quality decisions impacting product release and compliance.This role plays a critical part in:Supporting product commercialization and scale-upEnsuring sustained manufacturing complianceDriving continuous improvement across operationsMinimal travel as required.Qualifications/Training:Education: Bachelor's degree in science or related field required. Master'sdegree preferred.Minimum 10 years of relevant experience in Quality or Engineering in a medical device or regulated industryStrong working knowledge of:ISO 13485FDA 21 CFR Part 820Risk Management (ISO 14971)Experience with:CAPA and nonconformance systemsProcess validation and statistical analysisLean Six Sigma methodologies (Green Belt or Black Belt preferred)Demonstrated ability to:Lead and work with cross-functional teamsInfluence decision-making without direct authorityCommunicate effectively with internal stakeholders and external auditorsExperience with MES, statistical software, or data visualization tools (Minitab, Power BI, AI)All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.The estimated salary range reflects an anticipated range for this position is between $95,200-$128,800. The estimated salary range reflects an anticipated range for this position .The actual base salary offered may depend on a variety of factors.U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.To learn more please read Bausch + Lomb's Job Offer Fraud Statement.Our Benefit Programs: Employee Benefits: Bausch + LombApplicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.#LI-KF