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Validation Engineer - Job Opportunity at Jabil Circuit

Waterford, Ireland
Full-time
Mid-level
Posted: April 7, 2025
On-site
EUR 55,000 - 75,000 annually based on Ireland's medical device sector standards and role requirements

Benefits

Comprehensive healthcare package typical of multinational corporations
Professional development and training opportunities
Global career mobility across 100+ sites
Employee wellness programs
Competitive benefits package aligned with medical device industry standards

Key Responsibilities

Lead validation documentation and execution for medical device manufacturing processes
Ensure regulatory compliance with HPRA and FDA requirements
Drive cross-functional validation initiatives and quality management
Develop and execute validation master plans
Conduct GMP audits and risk assessments
Coordinate with external vendors on validation requirements
Implement quality management systems and compliance measures

Requirements

Education

Degree in Engineering/Science discipline

Experience

3 to 5 years in a Validation or Quality engineering role

Required Skills

Strong working knowledge of validation and quality principles Knowledge of EudraLex, ISO13485, ISO14644, GAMP5 FDA Pharma and medical devices regulations expertise Technical report writing Time management Computer & presentation skills Interpersonal and communication skills LEAN 6 sigma tools proficiency
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Sauge AI Market Intelligence

Industry Trends

Medical device manufacturing is experiencing increased regulatory scrutiny, particularly in EU markets with MDR implementation Growing emphasis on digital validation processes and computerized system validation in pharmaceutical manufacturing Rising demand for validation engineers with combined medical device and pharmaceutical expertise Increased focus on risk-based validation approaches aligned with latest FDA and EU guidelines

Role Significance

Typically part of a 5-10 person validation team within larger quality organization of 30-50 professionals
Mid-level position with significant responsibility for quality assurance and regulatory compliance, reporting to Quality Management leadership

Key Projects

Medical device manufacturing process validation Equipment and facility qualification programs Quality management system implementation Regulatory compliance initiatives Cross-functional process improvement projects

Success Factors

Strong understanding of both medical device and pharmaceutical regulatory requirements Ability to balance technical expertise with cross-functional collaboration Excellent documentation and technical writing capabilities Strong project management and organizational skills Proactive approach to compliance and quality management

Market Demand

High demand with steady growth projected due to expanding medical device manufacturing sector in Ireland and increasing regulatory requirements

Important Skills

Critical Skills

Regulatory knowledge (FDA, HPRA, ISO) is essential for ensuring compliance and product approval Process validation expertise directly impacts product quality and manufacturing efficiency Risk assessment capabilities are crucial for modern validation approaches Technical writing skills are fundamental for documentation requirements

Beneficial Skills

Project management skills enhance cross-functional coordination LEAN Six Sigma knowledge supports process improvement initiatives Industry 4.0 and digital validation knowledge becoming increasingly valuable Experience with multiple regulatory frameworks provides career flexibility

Unique Aspects

Opportunity to work with both medical device and pharmaceutical validation requirements
Exposure to global manufacturing networks and best practices
Combination of technical validation and quality system responsibilities
Strong focus on innovative manufacturing solutions

Career Growth

2-3 years in role before advancement opportunity, depending on project success and regulatory expertise development

Potential Next Roles

Senior Validation Engineer Validation Manager Quality Systems Manager Regulatory Affairs Manager Manufacturing Quality Lead

Company Overview

Jabil Circuit

Jabil is a global manufacturing solutions provider with over 50 years of experience and 100+ facilities worldwide

Top 3 electronic manufacturing services provider globally with strong presence in medical device manufacturing
Strategic location in Ireland's medical device manufacturing hub with significant investment in capabilities
Fast-paced, quality-focused environment with emphasis on continuous improvement and professional development
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