Information about #32870 Manufacturing Engineer

Work Location: Cuyahoga Falls, Ohio; there is some opportunity for remote work on a weekly basis

For more than 80 years, our company 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.

We look for people who are inclusive, results driven, customer-focused, and passionate about impacting the health and well-being of people, businesses, and communities around the world. If this inspires you, please join us at Clorox Purell.

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 company 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 handoff

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 team members as needed

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

GOJO Industries, Inc.

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