Senior QA Systems & Compliance Manager

PE Global (UK); Cork; On-site; EUR 120,000 - 150,000; Full time

Job summary

PE Global are recruiting for a QA Systems & Compliance Technical Manager for a leading pharmaceutical company in Cork, Ireland. This is a 12-month contract role with responsibility for overseeing quality systems, compliance, and regulatory readiness across the site.

The role requires extensive GMP experience, strong leadership, and the ability to drive cross-functional improvements while ensuring alignment with global processes. You will interact with stakeholders and participate in inspections.

Qualifications

• Bachelor's degree in Pharmaceutical Sciences or Process Engineering.
• 10–15+ years experience in GMP-regulated pharma/biotech.
• 3–5 years in leadership with cross-functional influence.
• Significant hands-on regulatory inspection experience.
• Knowledge of EU GDP Guidelines and regional regulations.
• Proven ability to lead change and mitigate risk.

Responsibilities

• Act as business process manager for QA systems.
• Assess GMP and regulatory risk areas; implement mitigations.
• Work with stakeholders to identify system improvements.
• Analyze performance through metrics and trending.
• Troubleshoot issues and support business queries.
• Benchmark leading practices and identify improvement opportunities.
• Liaise with global colleagues for consistency across network.
• Provide QA review/approval for Supplier Management and QMS activities (deviations, changes, specs, QAs).
• Support audit/inspection activities; lead site quality management review.

Skills

Quality systems

GMP compliance

Regulatory affairs

Leadership

Stakeholder mgmt

Risk assessment

Regulatory inspections

Cross-functional

Education

Bachelor's in Pharm Sci

Process Engineering

Job description

PE Global are recruiting for a QA Systems & Compliance Technical Manager for a leading pharmaceutical company in Cork, Ireland. This is a 12-month contract role with responsibility for overseeing quality systems, compliance, and regulatory readiness across the site.

The role requires extensive GMP experience, strong leadership, and the ability to drive cross-functional improvements while ensuring alignment with global processes. You will interact with stakeholders and participate in inspections.