Global R&D Quality Director
Listed on 2026-10-12
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Management
Regulatory Compliance Specialist
Estée Lauder Companies Inc. is one of the world’s leading manufacturers, marketers, and sellers of quality skin care, makeup, fragrance, and hair care products, and is a steward of luxury and prestige brands globally. The company’s products are sold in approximately 150 countries and territories under brand names including:
Estée Lauder, Aramis, Clinique, Lab Series, Origins, M
· A·C, La Mer, Bobbi Brown Cosmetics, Aveda, Jo Malone London, Bumble and bumble, Darphin Paris, TOM FORD, Smashbox, AERIN Beauty, Le Labo, Editions de Parfums Frédéric Malle, GLAMGLOW, KILIAN PARIS, Too Faced, Dr.Jart+, the DECIEM family of brands, including The Ordinary and NIOD, and BALMAIN Beauty.
Provide global leadership and management to ensure that proper policies/procedures are established to meet industry regulations and company business practices for both Quality Assurance and R&D. This includes all regulatory compliance requirements for change management and documentation control for OTC and cosmetics products globally.
Responsible for developing, implementing, and maintaining the corporate QA and R&D policies and procedures programs to ensure the company's quality reputation and regulatory compliance. In addition, manage the development and implementation of all corporate QA and R&D policy/procedure training as well as the technical writing associated with any document changes or new policies and procedures.
(50%):
- Responsible for leading the development and maintenance of a comprehensive set of corporate QA policies/procedures globally across QA, Supply Chain, and R&D.
- Works with QA/R&D Senior Management to ensure these global policies/procedures build on a community of best practices and meet all company and regulatory requirements.
- Leads a periodic policy/procedure review process that assures the policy requirements are current and applicable to regulations and business practices.
- Develops an effective document collaboration process that assures draft global documents are appropriately and adequately reviewed, edited, and approved.
- Leads and develops a two to three-year global policy/procedure strategy plan and every fiscal year develops an annual global document development plan that is approved by the QA/R&D leadership teams.
(30%):
- Responsible for developing and maintaining a comprehensive global training program for QA and R&D corporate policies/procedures.
- Assure personnel is adequately trained and that they understand the corporate policy/procedure requirements as well as ensure that they have the tools and knowledge necessary to perform their essential tasks.
- For approved global policy/procedure documents, ensure training records are documented and retained, including quizzes that demonstrate training effectiveness.
(15%):
- Manage and maintain the corporate part of the Open Text documentation software program that allows for the routing, tracking, approval, change control, and retention of both corporate QA/R&D global policies/procedures.
- Oversee the security, access, and upgrades to the Open Text software system.
(5%):
- Directly supervise and manage the Technical Writer position to assist in the development and implementation of the R&D policy/procedure documents program.
- Advanced level MS Office skills (particularly MS Word). Skills in a range of industry DTP Software.
- Professional understanding of templates, macros and styles.
- Must be detail-oriented and able to work with a high volume of documents in a fast-paced environment.
- Must be highly organized and process-oriented.
- Must have excellent oral, written communication and listening skills as well as the ability to interact and influence with all levels of the organization.
- Must be able to handle multiple requests while detailing…
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