QA Engineer, Third-Party Manufacturing (Hybrid)

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

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Company-paid life insurance

Company-paid short-term disability

Long-term disability

Supplemental life insurance

Flexible spending accounts

Critical illness insurance

Group legal

Job summary

Revlon Manufacturing & Distribution in Kenilworth, NJ is seeking a Quality Assurance Engineer to supervise third party manufacturing quality. You will develop and maintain QA protocols to ensure TPM supplier and product quality, and evaluate TPMs through audits and KPI tracking.

The role requires at least 3 years in supplier quality engineering, GMP/FDA knowledge, and hands-on experience with production processes.

Qualifications

• Bachelor or master’s degree in Biology, Chemistry, Engineering, or related fields.
• 3+ years of experience in supplier quality engineering or a similar role.
• Experience in Cosmetics, Food & Beverage or Pharma industries.
• Knowledge of GMP/FDA and quality management systems.
• Strong analytical and problem-solving abilities.

Responsibilities

• Evaluate TPMs and suppliers against product and schedule requirements.
• Develop and implement supplier quality evaluation and control systems.
• Manage TPM audits to reduce quality risks.
• Monitor TPM quality KPIs and drive corrective actions.
• Collaborate with TPMs and internal teams to implement quality improvements.
• Conduct TPM on-site audits and TPM qualification activities.
• Lead ATRs for new launches and manage TPM-related complaints.

Skills

GMP/FDA knowledge

Quality standards

Quality systems

Audit programs

Analytical skills

Communication skills

Autonomous

Travel willingness

Education

Bachelor or Master’s in Biology, Chemistry, Engineering

Job description

Revlon Manufacturing & Distribution in Kenilworth, NJ is seeking a Quality Assurance Engineer to supervise third party manufacturing quality. You will develop and maintain QA protocols to ensure TPM supplier and product quality, and evaluate TPMs through audits and KPI tracking.

The role requires at least 3 years in supplier quality engineering, GMP/FDA knowledge, and hands-on experience with production processes.