Global QA Policy & Training Leader

The Estée Lauder Companies

Melville (NY)

On-site

USD 120,000 - 180,000

Full time

8 days ago

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Job summary

The Estée Lauder Companies seeks a senior leader to oversee global QA policies and procedures for OTC and cosmetics, spanning QA, Supply Chain, and R&D. You will drive regulatory compliance, change control, and documentation management across the globe.

You will lead policy development, training programs, and a two-to-three-year strategy, while directing the OpenText documentation system and a technical writer to ensure accuracy and compliance.

Qualifications

  • Advanced level MS Office skills (particularly MS Word) and DTP software.
  • Templates, macros and styles knowledge.
  • Detail-oriented in a high-volume, fast-paced document environment.
  • Highly organized and process-oriented with strong communication.
  • Ability to interact and influence at all levels of the organization.
  • Experience in Quality Systems Management and documentation in regulated industries.
  • Minimum education BS/MS.

Responsibilities

  • Lead development and maintenance of global QA policies/procedures across QA, Supply Chain, and R&D.
  • Collaborate with QA/R&D senior management to meet regulatory requirements.
  • Oversee periodic policy review to stay current with regulations.
  • Develop document collaboration processes for review, editing and approval.
  • Lead 2–3 year global policy/procedure strategy and yearly development plans.
  • Develop and maintain a global QA/R&D training program and ensure training records.
  • Manage Open Text documentation system including routing, change control and retention.
  • Oversee Open Text security, access, and upgrades.
  • Directly supervise the Technical Writer to support policy/document programs.

Skills

MS Word
DTP Software
Templates & macros
Communication skills
Organizational skills

Education

BS/MS

Tools

Open Text

Job description

The Estée Lauder Companies seeks a senior leader to oversee global QA policies and procedures for OTC and cosmetics, spanning QA, Supply Chain, and R&D. You will drive regulatory compliance, change control, and documentation management across the globe.

You will lead policy development, training programs, and a two-to-three-year strategy, while directing the OpenText documentation system and a technical writer to ensure accuracy and compliance.

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