Quality Auditor-2

Quality Auditor-2

Job Description

Join the team behind iconic brands like Huggies®, Kleenex®, Cottonelle®, Scott®, Kotex®, Poise®, Depend®, and Kimberly-Clark Professional®.

 At Kimberly-Clark, it’s all here for you—innovation, growth, and the chance to make a real impact. 

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.

In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.

We are looking for a Quality Auditor provides on-shift support to Operations in regard to product specification and quality systems issues.

To provide laboratory tests for finished products and raw materials ensuring support to Operations. 

 

Key Responsibilities:

•        Perform work in a safe manner and responsible to follow 3 safety obligations.

•        Share expertise and knowledge of product quality and the consumer impact with operation's crews.

Coach Operations crew on product quality and ensure that operators focus on CTQ parameters and visual checks

•        Provide accurate and timeous testing results to identify and correct quality deficiencies on shift.

Conduct all performance tests as per required (WI-07666)

•        Attend daily shift hand over, production and QA meeting with CTQ report information and defected product samples.

•        Perform incoming packaging &corrugated case inspections and review documentation and determine disposition of key raw materials.

•        Complete NCR documents with additional investigation & test and send it to LCM to request supplier’s feedback.

•        Compiling of quality reports and accumulating quality statistical data, update QA board daily (RFT-Make, ppm etc.) and share daily CTQ report via e-mail with operation team.

•        Perform root cause analysis on out-of specification product with operation team.

•        Execute Quality Protocols and complete documentation, follow action plan.

•        Support R&E team with trials by performing relevant STM and providing results and recommendation to R&E

•        Complete KC 9001 Internal Audits as per Plant schedule and capture findings as CAPA’s on EtQ

•        Complete Board 0 Form for Finished Product non-conformances ensuring all required information is completed include 5WHY investigation and follow the NCP process (put sticker, complete Board0 report, update on hold /reject spreadsheet list dai...