Quality Assurance Engineer – TPMs (Hybrid, Cosmetics)

Revlon; Kenilworth (NJ); Hybrid; USD 83,000 - 103,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k plan

Vacation days

Holidays

Life insurance

Disability coverage

Flexible spending accounts

Identity theft protection

Job summary

Revlon, a global beauty company, seeks a Supplier Quality Engineer to manage TPMs, develop quality systems, and conduct on-site audits. The role focuses on ensuring product quality, supplier compliance, and continuous improvement across a dynamic cosmetics supply chain.

The position is hybrid, based in Kenilworth, NJ, requiring 3 days in-office with additional remote work. A strong background in QA, GMP/FDA, and cross-functional collaboration is essential.

Qualifications

• Bachelor or master’s degree in Biology, Chemistry, Engineering, or related field required.
• 3+ years in supplier quality engineering or similar role.
• Experience in Cosmetics, Food & Beverage or Pharma industries preferred.

Responsibilities

• Evaluate TPMs and suppliers for quality and schedule adherence.
• Develop and maintain supplier quality evaluation and control systems.
• Lead TPMs audits to reduce risk and ensure product quality.

Skills

Quality standards

GMP/FDA knowledge

TQM methodologies

Verbal and written communication

Autonomous

Auditor of Quality Systems

Travel as needed

Production processes

Attention to detail

Team player

Proactive problem-solving

Quality management systems

Organizational skills

Education

Bachelor or Master’s in Biology, Chemistry, Engineering or related

Job description

Revlon, a global beauty company, seeks a Supplier Quality Engineer to manage TPMs, develop quality systems, and conduct on-site audits. The role focuses on ensuring product quality, supplier compliance, and continuous improvement across a dynamic cosmetics supply chain.

The position is hybrid, based in Kenilworth, NJ, requiring 3 days in-office with additional remote work. A strong background in QA, GMP/FDA, and cross-functional collaboration is essential.