Manufacturing Ops Specialist: Quality & Process Improvement

Grifols, S.A; Dublin; On-site; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Pension scheme

Private medical insurance

Career development

Succession planning

Education allowance

Wellness initiatives

Job summary

Grifols, a global healthcare leader, is seeking a Manufacturing Operations Support Specialist in Dublin, Ireland. You will act as SME for operational support, drive deviations, CAPAs, change controls, and QRM, while ensuring compliance with cGMP and quality systems.

You will collaborate with Manufacturing, QA, Engineering, and Supply Chain to keep daily operations compliant and efficient, supporting continuous improvement and critical manufacturing needs.

Qualifications

• Bachelor’s degree in Science, Engineering, or related field.
• 1–2 years of GMP manufacturing or quality systems experience.
• Strong knowledge of cGMP and quality systems (deviations, CAPA, change control, QRM).
• Experience in technical writing and documentation.
• Experience in biologics or regulated pharmaceutical manufacturing is desirable.
• Lean / Six Sigma knowledge or experience is desirable.

Responsibilities

• Execute and support deviations, CAPAs, change controls, and QRM.
• Act as SME in one or more areas of operational support (investigations, documentation, training, or QRM).
• Support high-quality investigations with root cause analysis and corrective actions.
• Ensure tasks are completed accurately, on time, and compliant with procedures.
• Provide technical guidance to Operational Specialists; attend FAT or supplier visits if required.
• Collaborate with Manufacturing, QA, Engineering, and Supply Chain to resolve issues.

Skills

GMP manufacturing experience

Quality systems understanding

Technical writing

Problem solving

Attention to detail

Organizational skills

Education

Bachelor’s degree in Science/Engineering or related field

Job description

Grifols, a global healthcare leader, is seeking a Manufacturing Operations Support Specialist in Dublin, Ireland. You will act as SME for operational support, drive deviations, CAPAs, change controls, and QRM, while ensuring compliance with cGMP and quality systems.

You will collaborate with Manufacturing, QA, Engineering, and Supply Chain to keep daily operations compliant and efficient, supporting continuous improvement and critical manufacturing needs.