Laboratorios Farmacéuticos Rovi, S.A. is a leading Spanish pharmaceutical company engaged in the research, development, contract manufacturing, and commercialization of biological and small molecule medicines. As a member of the IBEX 35, the company operates on a global scale, particularly recognized for its leadership in the low-molecular-weight heparin (LMWH) market and its extensive contract development and manufacturing organization (CDMO) services.

Headquartered in Madrid, Rovi maintains a strong industrial presence with multiple production facilities across the Madrid region and Granada. For international professionals, Rovi offers diverse opportunities in high-tech manufacturing, quality assurance, and engineering, notably gaining global prominence through its strategic partnership with Moderna for fill-finish vaccine production. The company frequently recruits for technical and scientific roles, providing a gateway into the European pharmaceutical sector.

Founded in 1946 in Madrid by the López-Belmonte family, Rovi began as a small laboratory. It evolved into a global pharmaceutical group, going public in 2007 and eventually joining the IBEX 35 index in 2021.

For international professionals

Operates major manufacturing sites in Madrid (Alcalá de Henares, San Sebastián de los Reyes) and Granada.
Key global partner for Moderna, handling large-scale fill-finish operations for mRNA vaccines.
Publicly traded on the Spanish IBEX 35 index, indicating high corporate stability and scale.
Offers a wide range of 'Beca' (internship) programs, making it accessible for junior international talent and graduates.
Focuses heavily on R&D and specialized manufacturing, requiring diverse technical profiles from engineering to microbiology.

Compliance Quality Assurance Technician

Rovi

This job was originally posted in Spanish and automatically translated to English. You'll most likely need Spanish to apply.

Job Description

What do we do?

We are a Spanish pharmaceutical company engaged in the research and development, manufacturing and marketing of small molecules and biological medical products.

We likewise use our sales channels to market a number of licensed pharmaceutical products, imaging contrast agents and other products for hospital use, as well as OTC pharmaceuticals.

All of this is carried out through our specialized sales team formed by more than 260 people who promote the products with specialized medical professionals and in hospitals and pharmacies.

What will you do?

Perform on-site reviews at the manufacturing plant of the activities scheduled in the department to verify their correct execution in routine, and potential improvements in the CCS. Activities related to the manufacturing process of injectables such as:

Gowning processes in different types of classified areas,

Material disinfection process and flow

Aseptic practices of operations according to classification and activity

Execution of walkthroughs in the manufacturing plant, utilities, and laboratory

Detection of potential procedural non-compliances and/or activities for improvement.

Coordination with related areas and proposals for improvement mechanisms.

Your contract type will be:

Temporary (duración determinada)

The required education for the job is:

Technical Diploma: Biology

The experience for this job is:

From 1 to 2 years

View original advert (Spanish)

What do we do?

We are a Spanish pharmaceutical company engaged in the research and development, manufacturing and marketing of small molecules and biological medical products.

We likewise use our sales channels to market a number of licensed pharmaceutical products, imaging contrast agents and other products for hospital use, as well as OTC pharmaceuticals.

All of this is carried out through our specialized sales team formed by more than 260 people who promote the products with specialized medical professionals and in hospitals and pharmacies.

What will you do?

Realizar revisión en planta de fabricación de las actividades calendarizadas en el departamento para comprobar su correcta ejecución en rutina, y posibles mejoras en el CCS. Actividades relacionadas con proceso de fabricación de inyectables tales como:

Procesos de vestimenta en distintos tipos de areas clasificadas,

Proceso y flujo de desinfección de materiales

Prácticas asépticas de las operaciones según clasificación y actividad

Ejecución de walkthrough en planta de fabricaicón, utilities y laboratorio

Detección de posibles incumplimientos procedimentales y7o actividades mejorables.

Puesta en común con las áreas relacionadas y propuestas de mecanismos de mejora.

Your contract type will be:

Temporary (duración determinada)

The required education for the job is:

Technical Diploma: Biology