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.

Corporate QA Technical Specialist

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?

Management of Change Controls between the different plants of the group.

Plan and conduct internal and external audits to verify compliance with regulations.
Identify risk areas and propose corrective actions.
Maintain detailed and accurate records of all activities related to regulatory compliance.
Prepare reports on audit results and implemented corrective actions.
Evaluate and select suppliers based on their quality standards and regulatory compliance.
Conduct supplier audits to ensure compliance with quality requirements.

Management of Corporate documentation, as well as associated training.

Review and update QTAs with the company's clients.

Support during audits and inspections received at the different plants.

Your contract type will be:

Temporary (duración determinada)

The required education for the job is:

Bachelors Degree: Pharmacy (obligatorio), Masters Degree: Pharmacy

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?

Gestión de Controles de Cambios entre las diferentes plantas del grupo.

Planificar y realizar auditorías internas y externas para verificar el cumplimiento de las normativas.
Identificar áreas de riesgo y proponer acciones correctivas.
Mantener registros detallados y precisos de todas las actividades relacionadas con el cumplimiento normativo.
Elaborar informes sobre los resultados de las auditorías y las acciones correctivas implementadas.
Evaluar y seleccionar proveedores basándose en sus estándares de calidad y cumplimiento regulatorio.
Realizar auditorías a proveedores para asegurar el cumplimiento de los requisitos de calidad.

Gestión de la documentación Corporativa, así como los entrenamientos asociados.

Revisión y actualización de QTAs con los clientes de la compañía.

Soporte durante las auditorías e inspecciones recibidas en las diferentes plantas.

Your contract type will be:

Temporary (duración determinada)

The required education for the job is:

Bachelors Degree: Pharmacy (obligatorio), Masters Degree: Pharmacy