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 diversity adds value to our business, teams, and culture. We are committed to equal employment opportunities that foster an inclusive environment.

We are looking for a Quality Compliance Specialist to support Quality oversight of all day-to-day activities of the product lines with an emphasis on Supply Chain.

What your responsibilities will be

Principal accountabilities:

The specific duties/responsibilities include, but are not limited to:

• Responsible for Supplier Quality

• Supplier and Material Qualification

• Maintains the Quality Management system and ensures Quality Compliance especially for Supplier Quality related QMS documents

• Acts as backup and support Internal and external audit coordinator

Responsibilities

• Maintain and optimize the Quality Management System, including update and approval of QA documents

• Responsible for the supplier qualification and certification in cooperation with the purchasing department including supplier audit according to the risk based evaluation

• Supports the establishing and implementing the annual internal audit program

• Functions as internal auditor and supplier auditor

• Follow-up of corrective actions related to suppliers as well as internal/external audits/inspections.

• Management and follow-up of complaint investigations with suppliers, and of corrective actions related to supplier complaint investigations, and supplier audits/inspections

• Responsible for the administration of all registered documents including upload in the digital document management system, distribution and organization of periodic update.

• Initiate and follow-up of supplier-related change control, evaluate and perform impact assessment, risk assessment as well as control of the proper implementation and documentation of all changes

• Take part in / local lead for various projects and initiatives related to Quality Management System improvement

• Perform GMP inspection in production, warehouse and PTT lab area

• GTP back-office / Training assignation

• Follow-up of calibration plan

• Support of QA team and coordinator during audits/inspections

• Support of the Management Review including data collection

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www.grifols.com

Learn more about Grifols

Req ID: 525990

Type: Regular Full-Time

Job Category: Quality