Quality Control Reagent Laboratory Assistant

To successfully perform this job, a person must be able to carry out the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• You have a High School Diploma or possess a Vocational Training degree (CFGM/CFGS) in Analysis and Control or Clinical Diagnosis or similar training.
• You have 1 to 3 years of experience within the pharmaceutical, industrial, chemical sector, or similar.
• You have knowledge of GMP / GD&T regulations.
• You have experience with MS Office at a user level.
• You are an organized, meticulous person oriented toward quality, with the ability to work in a team and properly manage priorities.
• You stand out for your commitment, proactive attitude, and motivation to grow within a pharmaceutical environment.

• You have knowledge of SAP (Desirable).
• You have a B2 level of English (Desirable).

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

We believe that diversity adds value to our business, our teams and our culture. We are committed to equal opportunities and our mission is to provide an inclusive environment where differences add to our company.

Help us lead one of the largest pharmaceutical companies in the world. We are a global leader in plasma-derived medicines with a presence in more than 100 countries and a growing global team of more than 20,000 people. That is why we need for Diagnóstic Grifols a Reagents Quality Control Laboratory Assistant - Temporary to cover 4 hours in the morning shift, like you.

Guarantee the correct administrative functioning of the laboratory through document management, coordination with suppliers, and monitoring of equipment maintenance, ensuring adequate organization of resources, materials, and records, as well as compliance with established internal procedures.

• Manage and update the administrative documentation of the laboratory, ensuring the correct organization and traceability of information.
• Coordinate with external and internal suppliers the planning and monitoring of preventive and corrective maintenance of laboratory equipment.
• Ensure the correct functioning of maintenance equipment, incident management, databases, among others.
• Perform monitoring of incidents related to equipment and facilities, ensuring fluid communication with the involved areas and suppliers.
• Manage the reception, registration, and filing of technical documentation, certificates, maintenance reports, and other documentation associated with the laboratory.
• Support the management of material and supply orders, performing the corresponding administrative monitoring.
• Keep databases, records, and administrative inventory controls for the reagents area updated.
• Provide support in the coordination of access, technical visits, and actions by external companies within the laboratory.
• Ensure compliance with internal quality, safety, and document management procedures applicable to the area.
• Provide transversal administrative support to the laboratory team to guarantee the correct development of daily activity.

Schedule: 4 hours in the morning from Monday to Thursday 07:30 to 11:30 and Fridays 07:30 to 11:30.