QM Equipments & Facilities Specialist

Grifols; Parets del Vallès; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A global healthcare company is seeking a QM Equipments & Facilities Specialist in Parets del Vallès. This role involves ensuring that the critical production and quality control equipment meet regulatory standards. The ideal candidate has a degree in a related field, extensive experience in the pharmaceutical sector, and strong analytical skills. The position offers a flexible schedule, the option for remote work, and a full-time indefinite contract.

Servicios

Flexible schedule

2 days of remote work per week

Formación

• Advanced level of English – C1 is necessary.
• 3 years of experience in the pharmaceutical sector, sterile area is highly advantageous.
• Experience in GMP environments and basic statistics.
• Curious with strong analytical and synthesis skills.
• Ability to work in a collaborative and dynamic environment.

Responsabilidades

• Monitor and document incidents related to systems, facilities, and equipment.
• Oversee corrective or preventive actions from incidents.
• Prepare review reports based on collected data.
• Coordinate teams to communicate assessments.
• Review validation and qualification documentation.

Conocimientos

Analytical skills

Communication skills

Data-driven solutions

Educación

Bachelor’s degree in industrial engineering, Pharmacy, Biology, Chemistry, or related field

Master's or postgraduate degree in the pharmaceutical sector

Herramientas

MS Office

SAP

Descripción del empleo

Overview

Join to apply for the QM Equipments & Facilities Specialist role at Grifols.

Grifols is a global healthcare company with a presence in more than 110 countries and regions. We are a world leader in plasma-derived medicines and transfusion medicine. We are committed to equal employment opportunity and fostering an inclusive environment where diversity adds value to our business, teams, and culture.

Role mission

The main mission is to ensure that all critical production, quality control, and systems equipment are qualified, complying with requirements, regulatory standards (GMP, FDA, EMA), and internal policies.

Responsibilities

• Monitor and document incidents related to systems, facilities, and equipment.
• Oversee the follow-up of corrective or preventive actions arising from incidents.
• Analyze results trends.
• Prepare system, equipment, or facility review reports based on collected and analyzed data.
• Coordinate monitoring teams to communicate assessments and trends.
• Review documentation describing the operations and sampling of equipment and facilities.
• Review validation and qualification documentation associated with systems, equipment, and facilities.
• Prepare and submit documentation requested for audits conducted by national and international organizations and other companies.

Who You Are

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and / or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• Bachelor’s degree in industrial engineering, Pharmacy, Biology, Chemistry, or a related field.
• Master\'s or postgraduate degree in the pharmaceutical sector (valuable).
• Advanced level of English – C1 (necessary).
• 3 years of experience in the pharmaceutical sector, sterile area (highly advantageous).
• Experience in GMP environments and basic statistics.
• Knowledge of MS Office and SAP.
• Curious with strong analytical and synthesis skills, oriented toward data-driven solutions and continuous improvement.
• Strong communication skills and ability to work in a collaborative and dynamic environment.

What We Offer

Grifols offers opportunities for professional development in an excellent working environment. Information about Grifols is available at We are an equal opportunity employer.

• Flexible schedule: Monday-Thursday 7-16 and Friday 8-15 (with flexible start time).
• Contract of Employment: Indefinite Full Time.
• Flexibility for U Program: 2 days of remote work per week.
• Location: Parets del Vallès.

Job Details

• Seniority level: Mid-Senior level
• Employment type: Contract
• Job function: Engineering and Information Technology
• Industries: Pharmaceutical Manufacturing and Medical Equipment Manufacturing

Learn more about Grifols at

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