What are the responsibilities and job description for the Plasma Quality Assurance Specialist position at Grifols?
We are looking for a Plasma Quality Assurance Specialist who will be responsible for ensuring the quality and safety of our plasma-derived medicines. This includes overseeing all aspects of internal and external audits, including execution, documentation, review of responses, and implementation of corrective and preventative actions.
The ideal candidate will have a strong background in quality assurance and compliance, with experience working in a medical and/or cGMP regulated environment. You will be responsible for evaluating processes, developing action plans, and coordinating the strategic implementation of system processes and corrective actions.
You will also be responsible for leading projects and initiatives for the region and division, and will work closely with the Center Manager to develop the staff's knowledge of their job function and how their performance relates to the end product and patient.
This role requires strong analytical and problem-solving skills, as well as the ability to communicate complex information and ideas so others will understand. You must be able to work independently with minimal supervision and have a proven track record of maintaining high levels of quality and compliance.
