Process Excellence Manager — Cosmetic Launch & Manufacturing

L'oreal Usa; Clark (NJ); On-site; USD 90,000 - 129,000; Full time

Benefits offered by this job

Flexible time off

VIP shop discounts

Learning & development

Mentoring & career growth

Mental health & wellness

Summer Fridays

Volunteer time

Job summary

L’Oréal USA is seeking a Process Expert Manager within OMA to guide new product launches, assess risks with contract manufacturers, and support onboarding of new CM partners across global operations.

You will lead CM process validation, optimize bulk production, ensure compliance with ISO 9001/GMP, and drive continuous quality improvements through data review, CAPA, and cross-functional collaboration.

Qualifications

• Bachelor's degree in science or engineering, Chemical Engineering preferred.
• 4+ years of thorough experience in pilot lab, bulk lab, or related experience in process development.
• Experience in fast-paced consumer goods and cosmetics/personal care industry preferred.
• Knowledge of ISO Standards 9001 and GMP Standards (ISO 22716).
• Strong Excel skills.
• Leadership and management skills.

Responsibilities

• Prepare and manage technical dossiers for CM production costing.
• Review/Approve CM bulk manufacturing processes & bulk BOMs.
• Lead Process risk assessment with new and current CM.
• Train CMs to ensure understanding of process and manufacturing requirements.
• Provide technical support for all new launches and CM transfer.
• Manage quality waiver process and change control.
• Support audits and continuous quality improvement.

Skills

Leadership

Communication

Data interpretation

Excel skills

Attention to detail

Education

Bachelor's degree in science or engineering, Chemical Engineering preferred

Tools

Excel

Job description

L’Oréal USA is seeking a Process Expert Manager within OMA to guide new product launches, assess risks with contract manufacturers, and support onboarding of new CM partners across global operations.

You will lead CM process validation, optimize bulk production, ensure compliance with ISO 9001/GMP, and drive continuous quality improvements through data review, CAPA, and cross-functional collaboration.