Laboratory Assistant

Would you like to join an international team working to improve the future of the healthcare sector? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that since 1909 has been improving the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and we 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.

For Diagnostic Grifols S.A., an industrial company that researches, develops, and manufactures high-tech products for clinical diagnosis, we need to incorporate a Laboratory Assistant within the Quality Control department, for Reagent Quality Control.

Ensure the quality and reliability of laboratory analyses through the correct execution of analytical methods, compliance with regulations, and the traceability of results.

• You will execute the assigned analytical methods.
• You will be in charge of performing the laboratory's specific activities: sample analysis, reagent preparation, verifications, or tests assigned to you, following written control documents (analytical methods, specifications, instructions, calibrations, and equipment instruction manuals) while recording and electronically validating (if necessary) the results obtained.
• You will interpret the results obtained in the quality controls carried out by the laboratory, as well as ensure their recording and proper traceability and the investigation of anomalous results or incidents.
• You will perform the analysis of reagents and biological samples for internal use in the laboratory to ensure their traceability and material flows.
• You will ensure that instruments, materials, and/or reagents meet the defined requirements, and you will also be responsible for maintaining the correct order, maintenance, and cleanliness of the laboratory.
• You will know and comply with existing Quality (ISO, Internal Standards, GMP), Health and Safety, and Environmental Standards, as well as ensure their compliance.

Who you are

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 Vocational Training (CFGM/CFGS) with professional experience. Training in CFGS Analysis and Control or Clinical Diagnosis, or appropriate higher education, with a minimum of 1-2 years of experience in a Laboratory and knowledge of GMPs, will be positively valued.
• You have knowledge of MS Office, and knowledge of the SAP program at a user level is desirable.
• You possess the ability to work in a team, as well as initiative in the execution of your own tasks and problem-solving capacity when facing incidents and/or adversities.
• We will value if you have an FCE level of English.