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GLOBAL JOBS

The Estée Lauder Companies attracts the most outstanding people from diverse industries and nurtures their talents. Whether they work in one of our stores, on a production line, at our corporate headquarters in New York City or in one of our affiliates worldwide, our employees take pride in their contributions to our success.

Job Information

The Estee Lauder Companies Quality Control Manager TPM in Oevel, Belgium

Quality Control Manager TPM

Brand: Estée Lauder Companies

Description

Planning,

organizing, implementing and controlling the daily activities of the QC third

party laboratory to ascertain that components, raw materials, mass and finished

goods meet internal and external specifications. This for goods manufactured in

an EMEA Third party.

  • Responsible for overseeing lab testing processes with ability to troubleshoot instruments and issues.

  • Conduct and supervise all OOS investigations and reject investigations.

  • Manage QC lab equipment, qualification protocols, reports, and administration.

  • Participate in continuous improvement projects regionally to drive efficiencies in the lab.

  • Provide QC expertise to hygiene program and lead corrective action based on findings

  • Identify SOPs and support QC Lab Lead in work instruction updates or creating new based on lab trends and CAPAs.

  • Review SOPs and work instructions and provide to QC Lab Lead for approval.

  • First POC for Third Party QC questions.

  • Review of routine supporting test data and results, including sample preparation records, logbooks, calculations, and data sheets. Enter results in SAP/LIMS.

  • Ensure all lab processes are adhering to relevant regulatory GMPs and global company policies & procedures

  • Participate in in.ternal audits to ensure regulatory readiness

  • Monitor lab KPIs and drive improvements

  • Ensure all customer complaints are investigated, improvements implemented and response made in a timely manner

  • Assist in the development and execution of quality training curriculum for the laboratory

  • Collaborates on a daily base with supplier QA team.

Qualifications

  • 5 years of laboratory or packaging experience

  • At least 3 years in a supervisoryposition

  • At least 5 years of experience in packagingor product evaluation laboratories in Quality Control for a global consumergoods or pharma company

  • Experience in developing and revisinglaboratory SOPs

  • Strong knowledge of GMP, ISO and safetyguidelines

  • Knowledge of statistical assessments ofdata

  • Proficiency in Microsoft Office Suite, Electronic QMS, and SAP systemsis preferred

  • Flexible to support off-shift work when needed

Job: Supply Chain - Corporate

Primary Location: Europe, Middle East, Africa-BE-VAN-Oevel

Job Type: Standard

Schedule: Full-time

Shift: 1st (Day) Shift

Travel: Yes, 5 % of the Time

Job Number: 1921532

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