Quality auditor 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.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Quality Auditor Specialist like you.

Perform the planning, preparation, execution, follow-up, and closure of GMP audits, both internal and for plasma suppliers and related services, as well as the coordination of external audits (clients, certifying bodies, etc.) and regulatory inspections, ensuring proper documentation, regulatory compliance, and the continuous improvement of the quality system and the management of quality indicators within the area.

What your responsibilities will be

• Plan, prepare, execute and follow up internal and external cGMP audits.
• Generate study protocols, reports, and standard departmental documentation.
• Provide guidance and coordination to the team on specific work activities.
• Ensure knowledge and application of applicable working standards (GMP, SOPs, internal guidelines, GLP, etc.) in line with established procedures.
• Ensure accurate completion of records when required.
• Adhere to quality, safety, hygiene, and environmental regulations and standards.
• Report any incidents impacting normal operations to the direct supervisor.
• Perform tasks corresponding to lower professional levels when necessary.

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.

• Degree in Health Sciences (Pharmacy, Biology, Chemistry, Biochemistry, Biotechnology); Master’s and/or PhD desirable.
• Minimum of 2 years’ experience in the pharmaceutical industry.
• Knowledge of GMP, GLP, ICH, and related guidelines.
• Available to travel frequently (30%), both domestically and internationally, depending on audit projects.
• Advanced level English (C1) – indispensable.
• Strong time management and prioritization skills.
• Excellent communication, analytical skills, and attention to detail.
• Strong ability to work effectively within a team.

Benefits package

Flexible schedule: Monday-Thursday 8:00h – 17:00h and Friday 8:00 – 15:00h (with the same flexible start time).

Contract of Employment: Permanent position.

Grifols is an equal opportunity employer.