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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 integral 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 Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division of Instituto 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.

What your responsibilities will be





You will control and document incidents arising in production and control processes.
You will supervise the follow-up of corrective or preventive actions derived from incidents in production and control processes.
You will analyze data and trends from the processes.
You will prepare system review reports based on the collected and analyzed data.
You will coordinate follow-up groups to communicate process evaluations and trends.
You will review documentation that describes production operations and the functioning of equipment and facilities.
You will review qualification and validation protocols and reports.
You will prepare and deliver the documentation requested during audits and inspections conducted by national and international organizations and other companies.

Who you are

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of t

📌 Manufacturing Process Evaluation Specialist (Parets)
🏢 Grifols
📍 Parets