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 like you.
Misión del Rol
The role involves overseeing and conducting routine Good Manufacturing Practice (GMP) audits, as well as technical and specialized audits related to current products and potential licensing agreements. It also includes providing regulatory compliance guidance and support to the entire Quality organization, delivering training, and leading multidisciplinary teams and initiatives.
What Your Responsibilities Will Be
* Generate study protocols, reports, and standard departmental documentation.
* Review analytical results and related processes for assigned projects.
* 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 the audit projects.
* Advanced level of 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
* Flexibility for U Program: Remote working
* Location: Parets del Vallès
* Grifols is an equal opportunity employer.
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