Manufacturing Engineering, Other

Manufacturing Engineer

Formulated to Care For more than 75 years, GOJO, Makers of PURELL has been powered by people who are energized by helping the world experience greater health and well-being. The positive impact of our PURELL hand and surface hygiene solutions is driven by our global community of highly collaborative and talented team members who love to learn, innovate, care for each other, and deliver our Purpose of Saving Lives and Making Life Better.

Role Objective

The Manufacturing Engineer is responsible for providing a step change in operational effectiveness and efficiency in supply chain by developing, leading, and implementing engineering solutions focused on improving and optimizing the manufacturing and distribution processes within the GOJO Network. They are a highly collaborative subject matter expert that works cross functionally with multiple business units to drive operational excellence and achieve project objectives.

Essential Functions and Responsibilities

• Identify opportunities or implement changes to improve manufacturing, logistics, and distribution processes by improving performance, availability, quality, and other cost savings through material efficiencies, labor efficiencies, etc.
• Lead and manage engineering projects, either in capital execution or ongoing manufacturing and distribution continuous improvement, ensuring the successful execution and delivery of project objectives
• Leads and/or participates in continuous improvement initiatives utilizing industry standard tools and methods (Lean manufacturing/Six Sigma/Root Cause Analysis) to enhance manufacturing quality, reliability, or cost effectiveness through the use of OEE metrics.
• Participates in or leads redesign of equipment, facilities and processes for reduced costs, increased throughput, expanded capabilities and improved safety and regulatory compliance.
• Prepare and present project reports, including capital requests, trends and analysis related to manufacturing performance, process or equipment, project updates, budget analysis, and risk assessments to management and key stakeholders.
• Provides technical expertise and guidance for troubleshooting equipment, product, and process problems.
• Determine root causes of failures or recommend changes in designs, tolerances, or processing methods, using statistical procedures.
• Support planning, execution and maintenance of validation and cGMP documents for projects, equipment, or process modifications.
• Assure documentation is maintained in master Line Trial documents, IQ/OQ/PQ documents, and equipment files.
• Understands, develops, and leads technology transfer documentation, validation documentation and training of cGMP validation for new and modified OTC, EPA, drug, and other products and processes.
• Practices Project Management skills of project initiation, planning, execution, tracking, and control through to completion, and hand off.
• Coordinates project elements: scope, schedule, budget, quality, human resources, communications, and risks, ensuring adherence to project timelines and deliverables.
• Provides technical advice, training and mentoring for all GOJO employees.
• Translates tested or ambiguous concepts into design specifications for the manufacture and delivery of equipment.
• Design Specifications, standards URS, equipment type, components, and processes can become global standard for organization.
• Specifies, designs, obtains, and installs equipment and processes that supports GOJO organizational needs to produce finished products and services.
• Participate in feasibility studies for process safety and project risk assessments, identifying potential issues and implementing mitigation strategies.
• Collaborates with internal and external resources, vendors and suppliers to evaluate and implement new t