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QA Validation Engineer - Job Opportunity at PE Global

Sligo, Ireland
Contract
Mid-level
Posted: April 1, 2025
On-site
EUR 55,000 - 70,000 per year based on Irish pharmaceutical industry standards and role requirements

Benefits

Contract duration stability: 12-month term position
Experience with leading multinational pharma company
Professional development in GMP environment
Exposure to cutting-edge pharmaceutical validation processes

Key Responsibilities

Lead site validation program development and maintenance ensuring regulatory compliance
Coordinate quality assurance activities across equipment, utilities, processes and software
Develop and maintain validation master plans and documentation
Manage validation investigations and implement corrective actions
Oversee change control processes and validation equipment maintenance
Generate and review critical quality documentation and compliance reports

Requirements

Education

Qualification and/or degree in engineering or scientific discipline

Experience

3 years plus of knowledge of cGMP, validation and regulatory requirements

Required Skills

Strong communication (written and oral) Presentation skills Troubleshooting capabilities Effective interpersonal skills Organizational skills Independent work capability Team collaboration Work prioritization Multitasking ability
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on data integrity and electronic systems validation in pharmaceutical manufacturing Growing emphasis on continuous validation processes rather than point-in-time validation Rising demand for validation engineers with combined GMP and software validation expertise Trend toward integration of quality systems with digital transformation initiatives

Role Significance

Typically part of a 5-10 person validation team within a larger quality organization of 20-30 professionals
Mid-level position with significant responsibility for regulatory compliance and quality systems. The role carries substantial accountability for validation processes that directly impact product quality and regulatory compliance.

Key Projects

Implementation of new equipment validation protocols Software system validation projects Regulatory inspection preparation Quality system enhancement initiatives Validation program modernization efforts

Success Factors

Deep understanding of cGMP requirements and their practical application Ability to navigate complex regulatory requirements while maintaining operational efficiency Strong project management skills to handle multiple validation activities simultaneously Excellent documentation and technical writing capabilities for regulatory compliance

Market Demand

High demand position due to expanding pharmaceutical manufacturing presence in Ireland and increasing regulatory requirements. The role combines technical expertise with quality system knowledge, making it particularly valuable in the current market.

Important Skills

Critical Skills

GMP knowledge and application Validation protocol development Technical documentation Quality system management Regulatory compliance expertise

Beneficial Skills

Project management methodologies Risk assessment techniques Statistical analysis Computer system validation Change management expertise

Unique Aspects

Position offers exposure to multinational pharmaceutical operations
Opportunity to work with advanced validation methodologies
Complex role combining technical knowledge with regulatory expertise
Strategic location in Ireland's growing pharmaceutical sector

Career Growth

2-3 years in role before advancement, depending on performance and organizational growth

Potential Next Roles

Senior Validation Engineer Validation Manager Quality Systems Manager Regulatory Compliance Manager Technical Operations Manager

Company Overview

PE Global

PE Global is a significant recruitment firm specializing in technical and professional placements, particularly in the pharmaceutical and life sciences sectors

Well-established recruitment partner for major pharmaceutical companies in Ireland
Strong presence in Irish market with connections to major multinational pharmaceutical companies
Professional consulting environment with exposure to leading pharmaceutical companies and their quality systems
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  • Salary estimates and market demand analysis
  • Role significance and career growth potential
  • Critical success factors and key skills
  • Unique aspects of each position

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