Quality Control Manager — GMP/FDA Compliance

Kdc One; Saddle Brook (NJ); Presencial; USD 120.000 - 160.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Disability insurance

Life insurance

Paid vacation

Paid sick leave

Paid holidays

Performance bonus

Descripción de la vacante

Kdc One in New Jersey seeks a Quality Control Manager to lead QA/QC initiatives in cosmetics manufacturing. You will oversee inspections, laboratory testing, supplier quality, CAPA, and regulatory compliance with GMP, FDA, ISO standards, while driving continuous improvement.

The role requires strong leadership, rigorous documentation, and the ability to manage quality across materials, processes, and finished goods to ensure right-first-time production and audit readiness.

Formación

• Bachelor's degree in Science, Engineering or related technical discipline.
• Experience in quality control, manufacturing or operations within cosmetics/personal care.
• Proven ability in CAPA, audits, and regulatory compliance.

Responsabilidades

• Develop and maintain quality control procedures and quality systems.
• Ensure GMP, FDA, ISO compliance and customer requirements.
• Oversee QC inspections, testing, and material release decisions.
• Lead CAPA programs and investigations for non-conformances.
• Manage QC lab operations, calibration, methods, and staffing.
• Review supplier COAs and manage non-conforming materials.
• Maintain audit-ready quality documentation and reports.
• Drive continuous improvement and monitor key quality metrics.

Conocimientos

GMP knowledge

Quality control

Root cause analysis

Leadership

Communication

Analytical thinking

MS Office

Quality management software

Educación

Bachelor's degree in Science/Engineering

Herramientas

Quality management software

MS Office

Descripción del empleo

Kdc One in New Jersey seeks a Quality Control Manager to lead QA/QC initiatives in cosmetics manufacturing. You will oversee inspections, laboratory testing, supplier quality, CAPA, and regulatory compliance with GMP, FDA, ISO standards, while driving continuous improvement.

The role requires strong leadership, rigorous documentation, and the ability to manage quality across materials, processes, and finished goods to ensure right-first-time production and audit readiness.