Quality Engineering S

The 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.

Description The Quality Engineer II (QE II) is a leader within Quality Operations responsible for driving quality strategy, managing risk, and ensuring regulatory compliance across manufacturing operations at the Melville site.

This role leads complex investigations, advances risk mitigation and continuous improvement initiatives, and provides technical oversight across quality systems, validation, and new product launches. In addition to individual contributions, the QE II serves as a people manager, developing and leading a team, while strengthening technical capabilities in data analysis, statistical problem-solving, and quality engineering practices.

The QE II operates with a high degree of independence, influencing cross-functional and global initiatives to ensure sustainable process performance and a strong culture of quality.

Quality Investigations, CAPA & Risk Leadership (25%)

• Provide oversight and direction for consumer complaint, deviation, and quality inquiry (QI) investigations, and review investigation quality, trending, and effectiveness of corrective actions to prevent recurrence
• Lead complex, high-risk, and systemic investigations across manufacturing and packaging operations
• Apply advanced root cause analysis tools and ensure robust, risk-based CAPAs are developed and sustained
• Partner with site Quality leadership on significant quality issues originating within the Melville site

Work Center, Manufacturing & Packaging Technical Oversight (15%)

• Provide higher-level oversight and technical guidance for on-floor troubleshooting, manufacturing equipment challenges, and functional component issues
• Support escalation and resolution of quality-related disruptions impacting line efficiency and compliance
• Work with suppliers, developers, Packaging Development, Commercialization Engineering, and Production teams to define and align critical quality requirements

Advanced Data Analysis, Continuous Improvement & QE Projects (15%)

• Serve as a site resource for statistical process control (SPC), data analysis, and advanced trending methodologies
• Conduct and oversee analysis of data to identify trends, loss drivers, and improvement opportunities
• Lead or sponsor quality engineering projects using statistical tools and structured problem-solving methodologies
• Lead critical site quality initiatives and act as the Melville Site QA representative on global and cross-functional programs

New Product Launch (NPL), Validation & Process Excellence (20%)

• Provide quality leadership and oversight for NPL activities, including component evaluations, line tests, first production runs, in-process inspections, and post-trial evaluations
• Guide dFMEA and pFMEA activities and broader process mapping and risk mitigation efforts
• Collaborate with Commercialization Engineering, Packaging Development, Supplier Quality, Brand Quality, and cross-functional teams to identify and mitigate risks early in the product lifecycle
• Provide quality oversight for equipment URS development, qualification, and process validation (IQ/OQ/PQ)
• Serve as a GMP and compliance leader, ensuring activities align with internal procedures and global regulatory expectations
• Support internal audits and external inspections with strong technical and regulatory knowledge
• Act as a quality authority on documentation, procedures, technical reports, and quality records
• Drive audit readiness and compliance improvements across the site
• Support interpretation and application of regulatory requirements including FDA, ISO 22716, CSAR, and MFDS expectations

Lead, coach, and develop a small team of QE I roles and/or Quality Specialists

• Strengthen team capability in data analysis, statistical thinking, structured problem solving, and quality engineering practices
• Set priorities, allocate workload, and drive accountability for quality performance and deliverables

Provide technical mentorship and act as an escalation point for complex quality, validation, and risk issues

Qualifications Minimum Bachelor of Science degree in Engineering or Science, or equivalent experience (10+ years in a related field)

5% Travel

In addition to base salary, this position is eligible for participation in a highly competitive bonus program with the possibility for overachievement based on performance and company results.

In addition, The Estée Lauder Companies offers a variety of benefits to eligible employees, including health insurance coverage (medical, dental, and vision insurance), wellness and family support programs, life and disability insurance, retirement savings plans, paid leave programs, education-related programs, paid holidays and vacation time, and many others. Equal Opportunity Employer It is Company's policy not to discriminate against any employee or applicant for employment on the basis of race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. The Company will endeavor to provide a reasonable accommodation consistent with the law to otherwise qualified employees and prospective employees with a disability and to employees and prospective employees with needs related to their religious observance or practices. Should you wish to apply for this position or any other position with the Company and you believe you require assistance to complete an application or participate in an interview, please contact View email address on us.fitly.work.

Michigan Applicants: Persons with disabilities needing accommodations for employment must notify the company in writing of the need for an accommodation within 182 days after the date the person with a disability knew or reasonably should have known that an accommodation was needed.

Rhode Island Applicants: The company is subject to chapters 29-38 of title 28 of the general laws of Rhode Island and is therefore covered by the state's workers' compensation law.