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 employment opportunities that foster an inclusive environment.
We are looking for a Specialist Technician in the validation of computerized systems and Data Integrity for the Quality Control Division of Grifols SA, a company specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma.
Responsibilities: Make improvements to processes and general procedures in the Quality Control laboratories related to the validation of computerized systems, qualification of laboratory equipment, data integrity, risk analysis, etc.
Prepare periodic technical reports.
Participate in the preparation/review of validation documentation for computerized systems of laboratory equipment.
Provide support to the laboratories in activities related to data integrity.
Participate in the deployment of new procedures in the Quality Control laboratories.
Work in a GMP environment.
Who you are: Bachelor's degree in Biochemistry, Pharmacy, Biotechnology, or a similar field.
Experience related to Pharmaceutical Industry Laboratories and work in a GMP environment will be valued.
At least 2 years of experience in the validation of computerized laboratory systems in a GxP environment will be valued: development of system validation activities and preparation/review of validation documentation (VMP, AR, IQ, OQ, PQ, and other reports).
Knowledge of computerized system management: GAMP guidelines, 21 CFR Part 11, GMP Annex 11, etc.
Advanced level of English (First Certificate or higher).
Advanced knowledge of MS Office, especially Excel.
Knowledge of laboratory equipment software (Empower, Tiamo, Endoscan, or similar) will be valued.
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