Senior QC Lead - Global Pharma, Compliance & Growth

Grifols

Dublin

On-site

EUR 120,000 - 180,000

Full time

3 days ago
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Benefits offered by this job

Group pension
Private medical insurance
Wellness programs

Job summary

Grifols Worldwide Operations seeks a Senior Manager of Quality Control to lead QC activities, ensure GMP compliance, and drive continuous improvement across analytical testing and environmental monitoring. You will partner with cross-functional teams to support manufacturing, validation, and regulatory readiness.

The role emphasizes strong leadership, data integrity, and experience supporting regulatory inspections within a biotech/pharma setting.

Qualifications

  • Bachelor's degree in a scientific discipline relevant to GMP pharmaceutical manufacturing.
  • Significant GMP-regulated pharmaceutical/biotech experience.
  • Extensive experience leading Quality Control laboratory operations.
  • Proven leadership and people-management experience.
  • Strong knowledge of EU GMP, FDA regulations and data integrity.

Responsibilities

  • Provide leadership and strategic direction for Quality Control activities.
  • Oversee QC testing, environmental monitoring, and release support to manufacturing.
  • Ensure inspection readiness and effective regulatory submissions.

Skills

Leadership
Quality Control
GMP compliance
Data integrity
Regulatory inspections
Analytical testing
Cross-functional collaboration
Project management

Education

Bachelor's degree in Chemistry / Microbiology / Pharmaceutical Sciences
Advanced degree in a scientific discipline

Tools

Laboratory automation
Digital transformation

Job description

Grifols Worldwide Operations seeks a Senior Manager of Quality Control to lead QC activities, ensure GMP compliance, and drive continuous improvement across analytical testing and environmental monitoring. You will partner with cross-functional teams to support manufacturing, validation, and regulatory readiness.

The role emphasizes strong leadership, data integrity, and experience supporting regulatory inspections within a biotech/pharma setting.

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