Lead Quality Engineer
Lead Quality Engineer
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Position Purpose:
Provides Quality support to assigned Product Platform(s) at a manufacturing site.
Support includes site quality tasks such as change management support; investigation and resolution of non-conforming product and material events, significant consumer complaints, or other CAPAs; manufacturing data analysis; quality risk management; start-up protocol/process validation/verification planning; and routine problem-solving.
A significant focus of this role is on sanitary manufacturing support, including cleaning & sanitization validation, review of changes for sanitary impact, and analysis of process and environmental control data and its relationship to microbiological results.
Recommends and implements continuous improvement projects that support site quality & organization objectives.
Ensures compliance to established procedures and processes.
Customers:
Mill Operations, Regulatory Affairs, Product Safety, Research & Engineering, Packaging, Procurement, Legal, Component Suppliers, Product Supply.
In this role, you will:
* Demonstrate safety as a value by performing all job functions safely, while also complying with corporate policies and departmental procedures, in an effort to reduce risk and eliminate loss.
* Manage self in accordance with the expected behaviors of the Leadership Qualities.
* Effectively achieve results that meet business and individual objectives.
* Ensure activities and items are in compliance with both company quality assurance standards and applicable government regulations, such as GMPs and ISO requirements.
* Ensure that established manufacturing inspection, sampling and statistical process control procedures are followed as applicable.
* Performs production and quality systems audits.
* Maintain and demonstrate a high degree of knowledge and skill in product forms, quality systems, processes, and regulations.
* Establish and maintain good customer rapport, while driving solutions to meet business needs.
* Develop and maintain a strong spirit of partnership.
* Conduct all communications and transactions with the utmost integrity.
* Communicate fully with superiors, teammates, and others who have a need to know.
* Execute continuous improvement activities for established processes and initiates/supports development of new processes.
* Builds and maintains capability in QMS, ISO, and GMPs to support objectives.
Position Specifi...
- Rate: Not Specified
- Location: Beech Island, US-SC
- Type: Permanent
- Industry: IT
- Recruiter: Kimberly-Clark Corporation
- Contact: Not Specified
- Email: to view click here
- Reference: 879457
- Posted: 2025-06-19 08:50:52 -
- View all Jobs from Kimberly-Clark Corporation
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