Senior Project Engineer

Bausch + Lomb•US-FL-Tampa, FL

6d•Onsite

About The Position

As a Senior Project Engineer, 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.

Requirements

BS/MS Mechanical Engineering, Chemical Engineering, Material Science, Chemistry, Physics, or related technical discipline.
8+ years in Engineering and/or Construction Management.
Proven experience (5+ years) in managing large capital projects, 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.
Proficiency in project management tools/software (e.g., Planisware, Microsoft Project, Primavera) and MS Office suite.
Experience with facility renovation, construction, cleanrooms, clean and black utility systems, HVAC, manufacturing equipment start-up, and aseptic manufacturing operations.
Strong background with FDA and EU regulations.
Project management training or certification.
Strong communication and interactive skills, capable of leading and directing project teams as required.
Demonstrated ability to work across organizational boundaries.
Excellent verbal, writing and computing skills.
Familiar with MS Office, MS Project, CAD and Navisworks.
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

Advanced degree or professional certification (e.g., PMP) preferred.

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.
Develop 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.
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.
Develop 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.