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.
Mission
We are hiring a Global QA Specialist to join our Diagnostic Global Quality department. This role will be responsible for managing the Global Quality of our in vitro diagnostic medical devices manufacturing plants.
What your responsibilities will be
- Harmonize the Quality Management System across different Grifols Diagnostic in vitro diagnostic medical devices manufacturing plants.
- Ensure compliance with Corporate Grifols Quality policies and procedures.
- Support Quality Compliance, including audits and inspections, Distribution Quality Management, third‑party evaluation and monitoring and QMS implementation and maintenance.
- Establish Data Integrity policies and procedures.
- Create and maintain Global SOPs for Quality Management.
- Implement and manage Global Quality Management System software tools (Document Controls, Non‑Conformities, CAPA, Change Control, etc.).
- Establish, collect, and analyze Quality Key Performance Indicators (KPI).
- Perform internal and supplier audits.
- Establish and maintain Distribution Quality Management processes and Good Distribution Practices (GDP) for Grifols Diagnostic products.
- Manage Non‑Conformities, CAPA, and Change Control affecting different manufacturing plants or General Quality processes.
- Evaluate Quality Regulations to assess their impact on the QMS and establish implementation plans to ensure compliance.
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 the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- You have a Bachelor’s degree in Health Sciences or Engineering.
- At least 2 years of experience in a similar role, preferably in IVD medical devices Quality Management.
- You have a strong background in quality processes within medical devices or pharmaceutical industries.
- You have advanced Spanish and English communication skills.
- You can work effectively both independently and as part of a team.
- You have availability to travel occasionally.
What we offer
It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!
We look forward to receiving your application!
Grifols is an equal opportunity employer.
Flexibility for U Program: Hybrid Model
Benefits package
Contract of Employment: Permanent position
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