Global Quality Systems & Compliance Leader

Grifols, S.A; Dublin; Hybrid; EUR 90,000 - 120,000; Full time

Benefits offered by this job

Share options scheme

Group pension with company matching

Private Medical Insurance

Education assistance

Wellness and social activities

Job summary

Grifols in Dublin seeks a Manager to lead the site's Quality Systems & Compliance programme, ensuring conformity with regulatory and corporate requirements and protecting patient safety.

You will oversee QMS processes, data integrity, regulatory inspections, and cross-functional collaboration. The role includes driving CAPA, training, and supplier quality activities to sustain a high standard of quality across the site.

Qualifications

• Bachelor's degree in Science, Engineering, Pharmacy or related discipline.
• Significant experience in a regulated pharmaceutical/biotech/healthcare manufacturing environment.
• Strong knowledge of GMP requirements and data integrity principles.
• Experience managing quality systems including Change Control, Deviations, CAPA, Document Control, Training, and Supplier Quality.
• Experience supporting regulatory inspections and audit programmes.
• Previous leadership experience is desirable.

Responsibilities

• Lead and advance the site's Quality Management System and Compliance programme.
• Oversee Data Integrity activities and SOP governance across the site.
• Support regulatory inspections, audits and corrective actions.
• Coordinate cross-functional activities with Manufacturing, Engineering, Regulatory Affairs and Supply Chain.
• Coach and develop Quality Systems & Compliance personnel and promote a culture of accountability and continuous improvement.

Skills

GMP knowledge

Data Integrity

Leadership

Communication

Multi-priority management

Education

Bachelor's degree in Science, Engineering, Pharmacy

Tools

SAP

QMS software

Job description

Grifols in Dublin seeks a Manager to lead the site's Quality Systems & Compliance programme, ensuring conformity with regulatory and corporate requirements and protecting patient safety.

You will oversee QMS processes, data integrity, regulatory inspections, and cross-functional collaboration. The role includes driving CAPA, training, and supplier quality activities to sustain a high standard of quality across the site.