Quality Assurance Specialist

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 Assurance Specialist to join Quality Assurance area of Instituto Grifols SA, a company specialized in the research, development and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma.

What your responsibilities will be

- Oversee and ensure the effectiveness of the company's quality management system, fostering a culture of continuous quality improvement.
- Monitor key quality indicators and conduct comprehensive evaluations of the company's quality system.
- Propose and implement continuous improvement initiatives related to quality processes and systems.
- Manage the implementation and follow‑up of corrective and preventive actions (CAPA) to address quality issues.
- Coordinate and supervise the Quality Risk Management (QRM) process to proactively identify and mitigate potential risks.
- Lead and oversee global quality projects, ensuring alignment with organizational standards and objectives.
- Prepare and coordinate inspections with certification bodies and regulatory authorities to ensure compliance.
- Evaluate and monitor the quality systems of suppliers in accordance with current regulatory standards and company policies.
- Ensure that all materials involved in manufacturing processes meet established quality specifications.
- Verify that outsourced activities comply with the company's quality requirements and standards.
- Prepare and present Product Quality Review (PQR) reports in accordance with regulatory and internal standards.
- Manage quality agreements between Instituto Grifols SA and third‑party vendors to ensure adherence to required quality standards.

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 Science field (Biology, Chemical, etc).
- Minimum 2 years of experience in a similar position within pharma sector.
- High knowledge in GMP.
- English: Advanced level.
- High knowledge in MS Office.
- SAP user or similar ERP.
- You have excellent communication skills.
- You have the ability to analyze in an agile and decisive way.
- You are able to expose the issues in a clear and organized way focused on the objective.
- You have the ability to work as part of a team.

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 atwww.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

Flexible schedule:Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexibility start time).

Benefits package

Contract of Employment: Permanent position

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