Job Details

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. Our mission is simple, yet powerful: helping you see better, to live better.

Location: Greenville, South Carolina, United States
Date: Nov 6, 2025

Job Purpose

The Principal Equipment Process Engineer will provide leadership and support of critical, value‑added initiatives aligned with site priorities to implement variety of engineering projects for Lens Care Solutions manufacturing to increase machine efficiency and OEE, reduce cost, improve quality, and address critical obsolescence issues. Specify, design, and implement a portfolio of projects requiring cross‑functional partnering across multiple disciplines within the organization.

Key Activities

• Lead improvement projects and support daily operation of process equipment systems including packaging line equipment (cartoners, bundlers, case‑packers, palletizers, printers, labellers, vision systems, robotics). Diagnose and resolve complex manufacturing technical issues and develop technical solutions to improve process performance, quality, and cost. Engage cross‑disciplined resources to implement improvements aligned with site priorities.
• Develop and lead engineering projects designed to reduce waste, improve process capability, process reliability, increase OEE, improve quality, and manage capacity as required. Develop data acquisition and performance measuring techniques to gather and analyse critical data necessary to execute actions that improve product cost, quality, and manufacturing reliability.
• Manage engineering projects including scope, resource planning, budget activities, validation, and project execution timeline. Communicate status of project milestones to key stakeholders.
• Advise management of new developments which may affect profit, schedule, costs, customer relations, and/or inter‑departmental relations.
• Maintain a working knowledge of new technologies and develop recommendations and plans accordingly. Identify innovative technical and process solutions that drive the desired performance in cost, quality, compliance, customer service and revenue.

Qualifications

Education: BS or MS degree in Mechanical, Industrial, Electrical, or Manufacturing Engineering. Advanced degree preferred.

Experience: Minimum 10 years of relevant industrial experience in Pharmaceutical or Medical Device regulated manufacturing engineering with emphasis on Process & Packaging Equipment Design, process improvements, and GMP CapEx execution. Lean 6‑Sigma Green Belt certification or equivalent, PMP a plus.

Required Experience / Skills:

• Proven experience in manufacturing Process and Packaging equipment design and technology improvements in a GMP environment.
• Strong technical leadership capabilities with a proven ability to develop clear project objectives and work well in multi‑disciplinary teams to solve complex problems. Proven track record of delivering to objectives.
• Solid analytical and problem‑solving skills. Demonstrated proficiency in use of Process Excellence and Lean tools and Design for Six Sigma DFSS tools (DMAIC, DOE, VSM, RCA, FMEA, etc.).
• Proven ability to work autonomously within a fast‑paced, multitasking environment and effective at working across organizational boundaries.
• Excellent verbal and written communication skills and ability to influence at all levels of the organization.
• Strong conflict resolution, teamwork and negotiation skills, with proven ability to influence without authority.
• Proficient with the Microsoft office suite of tools including Microsoft Project, Visio, etc.
• Working knowledge of CAD software (SolidWorks™) and GD&T concepts.

Benefits & Legal Statements

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.