Quality Assurance Specialist (R&D)

Revlon; Marbella; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in beauty and cosmetics is seeking a Quality System Manager to oversee quality assurance processes across Europe. The successful candidate will manage the Quality system, ensure compliance with GMP standards, and evaluate suppliers. With a dynamic work environment and hybrid model, this role offers competitive salaries and numerous benefits.

Servicios

Hybrid working model

Subsidized meals at the office

Free parking for employees

Formación

• Minimum 4 years of experience in Quality systems, preferably in cosmetics or pharma.
• Proficient in English and Spanish.
• Knowledge of GMP, FDA standards, and TQM methodology.

Responsabilidades

• Manage Quality system and ensure GMP compliance.
• Conduct internal and external audits for suppliers.
• Train personnel on Quality documentation system.

Conocimientos

Communication

Analytical Skills

Problem Solving

Teamwork

Autonomous Work Ethic

Educación

University degree in a technical discipline

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 includes some of the 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!

• Are you able to work in a hybrid model? 3 days at the office, 2 days from home.
• Do you eat at the office? We have a high percentage subsidized by the company!
• Free parking for employees!

And much more benefits with competitive base salaries!

POSITION OVERVIEW

• Manage the Quality system, ensuring consistency across Europe (production plants and R&D Center).
• Provide support in the validation and evaluation of suppliers and third-party manufacturers (TPMs).

ESSENTIAL DUTIES & RESPONSIBILITIES

• Ensure GMP compliance and prepare necessary training.
• Write, execute, and review all documentation related to the Quality system, keeping it updated.
• Train personnel on the Quality documentation system.
• Evaluate and validate suppliers and TPMs.
• Conduct internal audits (intercompany plants) and external audits to suppliers and TPMs.
• Assist in audits of our facilities by health authorities and other third parties or customers.
• Manage and investigate Quality incidents, out-of-spec (OOS) results, and external complaints.
• Manage internal and customer complaints promptly, ensuring investigations, CAPA implementation, and verification.
• Support product recalls or retrievals.
• Support the Change Management System.
• Review documentation regarding qualification of equipment, services, and systems.
• Manage calibration of measurement, test, and control devices.
• Participate in QA activities during new developments, transfers, or insourcing.
• Provide support for all QA basic functions for FDA compliance :
• Review batch files and release FDA finished goods.
• Follow tasks listed on SOP-QA-003.

EDUCATION & EXPERIENCE Education

• University degree in a technical discipline.
• Proficient in English and Spanish.
• Knowledge of Quality Standards.
• GMP / FDA knowledge.
• Knowledge of TQM methodology and process management.

Experience

• Minimum 4 years of experience in developing and maintaining a Quality system, with experience in sanitization in the food, cosmetic, or pharma industry.

COMPETENCIES

• Excellent verbal and written communication skills.
• Strong analytical and problem-solving skills, with the ability to identify root causes, recommend options, prioritize, and implement solutions.
• People skills and teamwork orientation.
• Autonomous work ethic.
• Experience as a Quality Systems auditor.
• Ability to travel as needed to support Revlon business initiatives.
• Hands-on experience in production processes.

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