QA Specialist
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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 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 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.
Responsibilities
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, QMS implementation and maintenance, etc.
* 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 Global Quality processes.
* Evaluate Quality Regulations to assess their impact on the QMS and establish implementation plans to ensure compliance.
Who You Are
* 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!
We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.
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 (with the same flexible start time).
Benefits Package
Contract of Employment: Permanent position
Location: Sant Cugat del Vallès
www.grifols.com
Location: SPAIN : España : Sant Cugat del Valles : [[cust_building]]
Learn more about Grifols
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Contract
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing and Medical Equipment Manufacturing
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