Would you like to join an international team working to improve the future of healthcare? 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.
Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing general team of over 20,000 people. That’s why we need a Validations Technician like you.
Role Mission In the Validations Department at Laboratorios Grifols, we need to recruit an Equipment and Process Validations Technician. Their primary role will be to manage and execute assigned validation projects in accordance with current regulations, ensuring the validity of production processes.
You will edit deviations and change control assessments associated with validations.
You will validate the plant, at the equipment and process level, throughout its various stages of design qualification (DQ), installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ), as well as cleaning validation (CV) and process performance qualification (PPQ).
You will generate and review primary data associated with assigned validations.
Minimum of 2 years experience in the area of validations or quality systems of the pharmaceutical industry (GMP) or ISO quality systems. (You have an level of English (minimum B2).
You are proficient in the Office suite and have basic SAP user skills.
Flexible schedule Monday-Thursday 8:00h – 17:00h and Friday 8:00h 15:00h.
Benefits Package Contract of Employment: Permanent position
Flexibility for U Program: 1 day remote working