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.
We are looking for a Quality Specialist to join Good Distribution Practice (GDP) Compliance department at Grifols SA.
This person will support the team and the Technical Management personnel of the company's commercial subsidiaries and/or internal or external partners in an international environment.
What your responsibilities will be Develop procedures, work instructions and manuals of global international scope.
Track affiliate quality KPIs and prepare reports, collect, review and compile data in Excel.
Review and monitor distributors' and subsidiaries' health licenses (bonafides).
Coordinate and update contracts, rates, and local medicine serialization requirements, ensuring that necessary contracts are signed and reviewed by the relevant department and that fees are paid where appropriate.
Request, coordinate, review and compile global information that Headquarters requests from subsidiaries (corporate responsibility report, Retention Policies, etc.).
Preparation of technical presentations (PowerPoint, etc.).
Provide technical support to subsidiaries in documentation systems and use of Quality System computer tools.
Provide support in the process of training in SOPs.
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.
Bachelor's Degree in Life Sciences field (Pharmacy, Chemistry or similar).
Master's degree in Pharmaceutical Industry or a related area is a plus.
Experience in a similar role within pharma industry and/or medical devices.
Knowledge of regulations in the Quality field, such as GDP.
Advanced level of English.
Proficient user of Microsoft Office.
Knowledge of SAP is valuable.
You are meticulous and detail-oriented.
You have excellent communication and teamwork skills, as well as initiative and results orientation.
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 Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Benefits package Contract of Employment: Temporary position #J-18808-Ljbffr