Quality Engineer III
About The Position
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. 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.
Requirements
- Bachelor's degree in science or related field required.
- Minimum 10 years of relevant experience in Quality or Engineering in a medical device or regulated industry
- Strong working knowledge of: ISO 13485, FDA 21 CFR Part 820, Risk Management (ISO 14971)
- Experience with: CAPA and nonconformance systems, Process validation and statistical analysis, Lean Six Sigma methodologies (Green Belt or Black Belt preferred)
- Demonstrated ability to: Lead and work with cross-functional teams, Influence decision-making without direct authority, Communicate effectively with internal stakeholders and external auditors
- Experience with MES, statistical software, or data visualization tools (Minitab, Power BI, AI)
- Applicants 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.
Nice To Haves
- Master's degree preferred.
- Green Belt or Black Belt preferred.
Responsibilities
- Ensure compliance with qms requirements, including: Nonconformance (nc) management and capa systems, Change control and validation activities, Document review and approval (dhrs, sops, specifications)
- Provide quality oversight for: Contact lens product lifecycle, Process validation (sat/fat/iq/oq/pq/pv), Statistical sampling plans and data analysis, Design transfer activities in accordance with design control requirements
- Drive root cause investigations using structured methodologies: Pdca, 5y, dmaic, 8d, fishbone, etc. Ensure timely and effective containment, correction, and prevention
- Perform data analysis and trending to: Identify emerging risks and quality signals, Support decision-making through statistical tools
- Lead risk management activities aligned with iso 14971, including: Pfmea development and maintenance, Risk assessment, mitigation, and verification
- Act as a quality lead for continuous improvement initiatives: Reduce scrap, defects, and cost of poor quality (copq), Improve manufacturing capability and process robustness
- Ensure audit readiness and participate in: Internal audits, External regulatory inspections (e.g., fda, notified bodies)
- Collaborate with cross-functional teams (manufacturing, engineering, R&D, supply chain) to: Resolve quality issues, Support product lifecycle activities, Ensure alignment with design and regulatory requirements
- Mentor junior engineers, quality technicians and provide technical guidance to operations personnel and peers
Benefits
- medical, dental, vision insurance
- disability and life insurance
- a 401(k) plan and company match
- a tuition reimbursement program (select degrees)
- company holidays
- well-being benefits
- sick time
- floating holidays
- paid vacation
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
