GMP Quality Systems Specialist - Compliance & Audits

Grifols, S.A; Dublin; On-site; EUR 65,000 - 75,000; Full time

Benefits offered by this job

Highly competitive salary

Group pension scheme

Private medical insurance

Career development opportunities

Internal promotions

Wellness activities

Job summary

Grifols, S.A. is seeking a Quality Systems Specialist to maintain and continuously improve the site's Quality Management System (QMS). You will manage document control, change controls, CAPAs, supplier qualification, supplier complaints, GMP training, and internal audits.

Join a global healthcare team focused on EU and FDA GMP compliance, inspection readiness, and quality excellence across the site. You will collaborate cross-functionally with Quality, Manufacturing, Engineering, and Supply

Qualifications

• Bachelor's degree in Science, Pharmacy or related discipline.
• 2+ years in a GMP pharmaceutical quality systems environment.
• Experience with change controls, CAPAs, deviations, supplier qualification and supplier complaints.

Responsibilities

• Maintain the site's Quality Management System (QMS) documentation and DCM system.
• Prepare and distribute QMS reports, metrics, and compliance trends.
• Author, review, and maintain SOPs and other quality documentation.
• Coordinate and manage Change Controls, CAPAs, supplier qualifications, supplier performance reviews, and supplier complaints.
• Support internal audit programmes and regulatory inspections.

Skills

Quality systems

GMP knowledge

Change controls

CAPAs

Supplier qualification

Audits

Documentation

Education

Bachelor's degree in Science/Pharmacy

Tools

Microsoft Office

Job description

Grifols, S.A. is seeking a Quality Systems Specialist to maintain and continuously improve the site's Quality Management System (QMS). You will manage document control, change controls, CAPAs, supplier qualification, supplier complaints, GMP training, and internal audits.

Join a global healthcare team focused on EU and FDA GMP compliance, inspection readiness, and quality excellence across the site. You will collaborate cross-functionally with Quality, Manufacturing, Engineering, and Supply