Qa Operations Manager

Estée Lauder Companies

Petersfield, United Kingdom
On-site
Gmp and regulatory compliance knowledge
Root cause analysis and capa implementation
Team leadership in manufacturing environment
Estée Lauder Companies is seeking a Quality Operations Manager to oversee Quality Assurance on the night shift at their Whitman Laboratories in Petersfield, UK. The role involves ensuring compliance, driving continuous improvement, and managing a team to support high-quality production across various operations

Job Summary

  • This role leads Quality Assurance activities across incoming materials, manufacturing operations, and new product introductions at a site responsible for a fifth of the company's global sales.
  • The successful candidate will manage a team of specialists, drive continuous improvement initiatives, and ensure strict compliance with GMP and regulatory standards.
  • Key responsibilities include leading deviation investigations, overseeing customer complaint resolutions, and supporting high-quality production across the plant.

Matching Summary

Match Score: 85

Estée Lauder Companies is seeking a Quality Operations Manager to oversee Quality Assurance on the night shift at their Whitman Laboratories in Petersfield, UK. The role involves ensuring compliance, driving continuous improvement, and managing a team to support high-quality production across various operations.

Skills & Requirements

Must-have

  • GMP and regulatory compliance knowledge
  • Root cause analysis and CAPA implementation
  • Team leadership in manufacturing environment
  • Deviation investigation and OOS disposition
  • Continuous improvement and RFT performance

Nice-to-have

  • Experience with cosmetics or pharmaceuticals
  • Statistical sampling (AQL/ANSI) expertise
  • Cross-functional stakeholder influence skills
  • SAP and electronic QMS proficiency
  • Training and coaching capability

Key Requirements

  • Proven experience in fast-paced manufacturing environment
  • Strong working knowledge of GMP and ISO 22716/FDA standards
  • Demonstrated people management and team leadership capability
  • Experience with audits and quality systems documentation

Work Rights

Not specified

Tailored Resume

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