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.

New Projects 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?

Coordinate the activities of the Quality Control Laboratory associated with QC projects according to the needs and priorities of the department.

Ensure the correct sampling of materials, raw materials, or products when necessary for analysis or shipments to customers associated with projects.

Ensure that raw materials, packaging materials, intermediate products, and/or finished products are analyzed according to the indicated specifications, procedures, and protocols approved.

Supervise the analyses associated with projects carried out by the quality control analysts.

Control the stock of laboratory materials to be used in the area's projects and ensure they are used within their expiration period.

Ensure that results and operations are documented in a timely and proper manner in the specific notebooks / LIMS, in compliance with current regulations for the analysis and manufacture of medicines and the company's quality system.

Follow up on the results of sampling for area and service qualification exercises, related to environmental monitoring and water systems analyzed by the Quality Control laboratory of the SSRR plant or external subcontractors.

Perform Risk Assessment for the implementation of new manufacturing areas to establish environmental monitoring points

Develop protocols and reports for validation and verification methods for bioburden, TOC, and UPLC.

Ensure compliance with Quality regulations and internal requirements of the company's Quality system.

Ensure compliance with the company's Quality System together with the rest of the department.

Participate in necessary training activities, both for Quality Control personnel and other areas.

Daily monitoring of activities performed associated with projects, planning, and samples received in each shift.

Ensure compliance with standards and procedures established in the Quality system, as well as compliance with GMP regulations, guidelines (ICH), and pharmacopeias, relating to QC Project area activities.

Maintenance and updating of documentation related to the work area.

Participate in the development and review of guides, procedures, and protocols relating to QC Project activities.

Generate procedures and application documentation in the area: investigations, specifications, protocols and reports, validations, qualifications, transfers, and other documents subject to cGMPs regulation.

Establish plans, protocols, and reports associated with the qualification tasks of classified zones and utilities for water and gases.

Execute non-conformities, deviations, and corrective and preventive actions derived from the projects and qualification exercises in which they are part of the project team.

Coordinate relevant deviations and non-conformities, according to specific procedures, and draft investigations generated in Projects led by or with participation in the project team from the area.

Investigate in a timely manner all out-of-specification results or deviations that occur in the area.

Participation in audits and self-inspections related to matters of the area

Your contract type will be:

Temporary (fixed-term)

The required education for the job is:

Bachelors Degree: Biology (mandatory), Bachelors 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?

Coordinar las actividades propias del Laboratorio de Control de Calidad asociadas a proyectos de QC según las necesidades y prioridades del departamento.

Asegurar el correcto muestreo de materiales, materias primas o productos en caso necesario para análisis o envíos a clientes asociados a proyectos.

Asegurar que las materias primas, material de acondicionamiento, producto intermedio y/o producto terminado se analicen según lo indicado en las especificaciones, procedimientos y protocolos aprobados.

Supervisar los análisis asociados a proyectos realizados por los analistas de control de calidad.

Controlar el stock de los materiales del laboratorio que se deben usar en los proyectos del área y velar por que se usen dentro de su periodo de caducidad.

Asegurar que se documenta en tiempo y forma, en cumplimiento con normativa vigente de análisis y fabricación de medicamentos y sistema de calidad de la comparación los resultados y operaciones en los cuadernos específicos / LIMS.

Realizar seguimiento de los resultados de los muestreos de los ejercicios de cualificación de áreas y servicios, relacionados con monitorización ambiental y sistemas de agua analizados por el laboratorio de Control de Calidad de la planta de SSRR o externos subcontratados.

Realizar Risk Assesment para la implementación de nuevas áreas de fabricación para implementar los puntos de monitorización ambiental

Realizar protocolos e informes de métodos de validación y verificación de bioburden, TOC y UPLC.

Asegurar el cumplimiento de las normativas de Calidad y requerimientos internos del sistema de Calidad de la compañía.

Velar por el cumplimiento del Sistema de Calidad de la compañía juntamente con el resto del departamento.

Participar en las actividades de formación necesarias, tanto para el personal de Control de Calidad como de otras áreas.

Seguimiento diario de las actividades realizadas asociadas a proyectos, planificación y muestras recibidas, en cada turno.

Asegurar cumplimiento de estándares y procedimientos establecidos en el sistema de Calidad, así como el cumplimento de normativa GMP, guías (ICH) y farmacopeas, relativos a actividades del área de Proyectos QC.

Mantenimiento y actualización de la documentación relacionada con su área de trabajo.

Participar en el desarrollo y revisión de guías, procedimientos y protocolos relativos a actividades de Proyectos QC.

Generar los procedimientos y documentación de aplicación en su área: investigaciones, especificaciones, protocolos e informes, validaciones, cualificaciones, transferencias, y resto de documentos objeto de regulación cGMPs.

Establecerlos planes, protocolos en informes asociados a las tareas de cualificación de zonas clasificadas y servicios (utilities) de agua y gases.

Ejecutar las no conformidades, desviaciones y acciones correctivas y preventivas derivadas de los proyectos y ejercicios de cualificación en los que forme parte del equipo de proyecto.

Coordinar las desviaciones y no conformidades que procedan, según los procedimientos específicos, redactar las investigaciones generadas en los Proyectos liderados o con participación en equipo de proyecto desde el área.

Investigar a tiempo todos aquellos resultados fuera de especificaciones o desviaciones que se den en su área.

Participación en auditorias y autoinspecciones relacionadas con materias de su área

Your contract type will be:

Temporary (duración determinada)

The required education for the job is:

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