Quality Auditor-1 at Kimberly-Clark

About the position

The 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.

You will then need to apply and send your current updated CV, with confirmation of the below :

What will you be doing?

• Performing work in a safe manner and responsible to follow 3 safety obligations,
• Sharing 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
• Providing accurate and timeous testing results to identify and correct quality deficiencies on shift. Conduct all performance tests as per required (WI-07666)
• Attending daily shift hand over, production and QA meeting with CTQ report information and defected product samples.
• Performing incoming packaging & corrugated case inspections and review documentation and determine disposition of key raw materials
• Completing NCR (Non-Conformance report) documents with additional investigation & test and send it to LCM (Life Cycle Management) to request supplier’s feedback
• You’ll be Compiling quality reports and accumulating quality statistical data, updating QA board daily (RFT / Right First Time -Make, ppm etc.) and sharing daily CTQ report via e-mail with operation team.
• Performing root cause analysis on out of specification product with operation team
• Executing Quality Protocols and complete documentation, follow action plan
• Supporting R&E (Research & Engineering) team with trials by performing relevant STM (Standard Test Method) and providing results and recommendation to R&E
• Completing KC 9001 Internal Audits as per Plant schedule and capture findings as CAPA’s on EtQ
• Completing Board O Form for Finished Product non-conformances ensuring all required information is completed include 5WHY investigation and follow the NCP / Non-Conforming Product process (put sticker, complete Board O report, update on hold /reject spreadsheet list daily)
• Completing weekly calibration & verification with related equipment’s and record it on the same day, every Monday record should be checked by following shift.
• Completing monthly calibration & verification 1st week of the month and record it on the same day, record should be checked by following shift.
• Following up on the approved waivers and ensuring assets teams are updated
• Placing pictures/examples of key defects on the boards in QA part as ref, ensure they are updated at least Daily - track (QA) and report
• Supporting Mill Quality Manager with entrenching EtQ spec module use within Epping
• Conducting customer complaint analysis of samples & complete QA Ad hoc tasks
• Conduct Daily GMP for Epping Mill and send out the GMP findings daily

What are we looking for?

• A recognized qualification in Quality or National Diploma/Bachelor’s degree in food science, Microbiology and Chemistry
• Minimum of 1 to 2 years’ experience in a Manufacturing or relevant Quality role within a Fast-Moving Consuming Goods environment as a Quality Auditor.
• Computer Literacy
• Experience in ISO 9001 standards will be an advantage
• PASS System knowledge will be an advantage.
• Problem solving and analytical skills

Personal Skills

• Good command of English is a must,
• Strong organisational skills, effective at planning and able to manage and prioritise
• Highly collaborative, with exceptional attention to detail
• Strong interpersonal, communication and presentation skills
• Professionalism and resilient under pressure