Principal Engineer

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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/Purpose of Job:

As a Principal Engineer, Program/Project Manager, you will lead scope development, capital budget requirements, timelines, and the implementation of multi-year Site Master Plan (SMP) activities for complex business critical projects aligned with the Tampa Manufacturing site priorities.

Key Activities/Responsibilities:

• Develop and maintain a detailed project plan outlining key milestones, deliverables, timelines, and resource requirements for the SMP.
• Lead cross-functional teams in the identification, assessment, and prioritization of site infrastructure, facility and utility system upgrades, and process improvements needed to support current and future manufacturing operations.
• Lead individual capital projects (equipment or facility improvements) within the project portfolio from initial project definition and scope development, detailed project charter/scope, risk assessment, milestone schedule, budget, resource plans, user and functional requirements, conceptual design, detailed design, risk assessment, and equipment selection through start-up, commissioning, and qualification.
• Manage the budgets, spending forecasts, resources, and timelines for the SMP, ensuring adherence to financial targets and project milestones.
• Facilitate regular project status meetings, provide updates to senior leadership, and escalate issues with recommendations necessary to ensure timely resolution and project success.
• Collaborate with and lead external vendors, contractors, and consultants to support the design, estimating, construction, and commissioning of facility upgrades and new infrastructure.
• Ensure compliance with applicable regulatory standards, including FDA cGMP guidelines, EU GMP Annex 1, and other relevant regulations governing pharmaceutical aseptic manufacturing facilities.
• Drive continuous improvement initiatives to optimize manufacturing processes, increase operational efficiency, and enhance quality and safety standards.
• Develop and maintain strong relationships with internal stakeholders and external partners to foster collaboration, transparency, and alignment throughout the project lifecycle.
• Prepare and deliver presentations, reports, and updates to senior management, site leadership, and key stakeholders on project status, risks, and opportunities.
• Provide SME knowledge in areas such as construction management, design, installation, commissioning and qualification, troubleshooting of aseptic clean rooms, process equipment, process flows, clean and black utility systems in a pharmaceutical site to industry standards.
• Drive application of industry standards and best practices. Chair regular program meetings that include periodic internal B&L project managers meetings to monitor alignment and progress to plan. Identify any risks to deliverables and develop and implement risk mitigation plans as required.

Qualifications/Training:

• BS/MS Mechanical Engineering, Chemical Engineering, Material Science, Chemistry, Physics, or related technical discipline; 10-15 years in Engineering and Construction Management. Advanced degree or professional certification (e.g., PMP) preferred.
• Proven experience (10+ years) in managing large capital projects and/or programs, preferably within the pharmaceutical or biotechnology industry, with a focus on facility design, construction management, and operations.
• Strong understanding of aseptic manufacturing principles, cleanroom design, HVAC systems, and regulatory requirements for pharmaceutical manufacturing facilities.
• Demonstrated leadership skills with the ability to lead cross-functional teams, drive consensus, and manage multiple priorities in a fast-paced environment.
• Excellent communication, presentation, and interpersonal skills, with the ability to effectively engage and influence stakeholders at all levels of the organization.
• Strategic thinker with a results-oriented mindset, analytical capabilities, and a track…