First-Class Sterilization Operator

Being part of Grifols means the opportunity to work in an international environment where equal opportunities are promoted.

It means the opportunity to develop professionally, have continuous training, and integrate into a team of professionals where each individual's contribution counts. Our commitment is to maintain an environment that fosters the professional development of our employees in a good work atmosphere.

Grifols' human capital is key to both the development of activities and the company's expansion process.

We believe in diverse talent and want to eliminate any barrier that may prevent your participation. If you need any adjustment in our selection process, please do not hesitate to inform us when applying. We are here to help you.

• Schedule: 8h rotating shifts.
• Employment contract: Permanent.

Location: SPAIN : España : Parets del Valles:

Learn more about Grifols

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.

Join Grifols Laboratories!

For the company Laboratorios Grifols, S.A., specialized in the research and development of hospital products such as parenteral solutions, enteral and parenteral nutrition diets, and specific products for blood banks, the Production department requires the incorporation of a Sterilization Operator.

• You will execute, control, and verify sterilization processes, ensuring compliance with established procedures, manufacturing guides, and quality standards.
• You will manage the automatic basket system (MECTRA), guaranteeing the correct development of production processes.
• You will verify, before each process, that calibrations, validations, and preventive maintenance are up to date.
• You will start up, follow, and control sterilization cycles, reviewing reports and entering the corresponding data into SAP.
• You will perform cleaning tasks, equipment checks, and sampling valve changes according to current procedures.
• You will supervise the correct functioning of the MECTRA system: startup and shutdown, batch management, incident resolution, and alarm control.
• You will provide support to the Dosage, Packaging, R&D, and Validation departments during production tests or incidents.
• You will comply with working standards (GMP, SOP, HSE, GLP), as well as quality, safety, hygiene, and environmental standards.

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.