Quality Assurance Specialist (R&D)

Revlon; Madrid; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

Una empresa innovadora busca un profesional apasionado por la calidad para gestionar su sistema de calidad en Europa. En este emocionante rol, serás responsable de garantizar el cumplimiento de las normativas GMP y FDA, así como de evaluar y validar proveedores. Con un enfoque en la mejora continua y el trabajo en equipo, tendrás la oportunidad de influir en la calidad de productos icónicos en la industria de la belleza. Si tienes experiencia en sistemas de calidad y un deseo de marcar la diferencia, esta posición es para ti.

Formación

• Mínimo 4 años de experiencia en desarrollo y mantenimiento de un sistema de calidad.
• Conocimientos de estándares de calidad y metodología TQM.

Responsabilidades

• Gestionar el sistema de calidad, asegurando la consistencia en Europa.
• Realizar auditorías internas y externas a proveedores y TPMs.
• Gestionar incidentes de calidad y quejas externas.

Conocimientos

Comunicación verbal y escrita

Resolución de problemas

Trabajo en equipo

Conocimientos de GMP

Conocimientos de FDA

Habilidades analíticas

Educación

Título universitario en disciplina técnica

Herramientas

Sistemas de gestión de calidad

Descripción del empleo

At Revlon, we’re passionate about all things beauty and inspiring women to ‘Live Boldly’. Since the launch of the first opaque nail enamel in 1932, Revlon has provided our consumers with high-quality products that deliver sophisticated glamour. Today, Revlon's diversified portfolio of brands is sold in more than 150 countries around the world and has some of the world’s most iconic and desired brands in color cosmetics, skin care, hair care, hair color, and fragrances.

At Revlon, we are equally passionate about our team! We celebrate success, invest in health and wellbeing initiatives, as well as professional development programs designed to unlock potential.

In Barcelona, we are the second largest headquarters globally!

POSITION OVERVIEW

Manage the Quality system, ensuring consistency in Europe (production plants and R&D Center).

Provide support in the validation and evaluation of suppliers and third-party manufacturers (TPMs).

ESSENTIAL DUTIES & RESPONSIBILITIES

1. Ensure GMP Compliance and prepare necessary training.
2. Write, execute, and review all documentation related to the Quality system and keep it updated.
3. Train personnel on the Quality documentation system.
4. Evaluate and validate suppliers and TPMs.
5. Carry out internal audits (intercompany plants) and external audits to suppliers and TPMs.
6. Provide assistance to audits of our facilities by health authorities and other third parties or customers.
7. Manage and investigate Quality incidents and out of spec (OOS) as well as external complaints.
8. Timely management of internal and customer complaints to assure the necessary investigations have been made, and the necessary CAPA is applied and verified.
9. Provide support on product recalls or retrievals.
10. Provide support on the Change Management System.
11. Provide support and review documentation regarding qualification of equipment, services, and systems.
12. Manage calibration of measurement, test, and control devices.
13. Participate in QA activities during new developments, transfers, or insourcings.
14. Provide support on all QA basic functions for FDA Compliance:
15. Review the Batch file and release FDA finished goods.
16. Tasks listed on the SOP-QA-003.

EDUCATION & EXPERIENCE

Education:

1. University degree in technical discipline.
2. Proficient in English and Spanish.
3. Knowledge of Quality Standards.
4. GMP / FDA knowledge.
5. Knowledge of TQM methodology and processes management.

Experience:

Minimum 4 years of experience in developing and maintaining a Quality system as well as experience in sanitization in the food, cosmetic, or pharma business.

COMPETENCIES

1. Excellent verbal and written communication skills.
2. Excellent analytical and problem-solving skills with the ability to identify root-cause, recommend options, prioritize, and implement appropriate solutions.
3. Must have people skills and Team Work.
4. Autonomous.
5. Auditor of Quality Systems.
6. Ability to travel as needed to support Revlon business initiatives.
7. Real experience hands-on in production processes.
8. Experience in direct contact with customers.