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Senior Validation Engineer - Job Opportunity at ICDS Recruitment Consultants

Dublin, Ireland
Full-time
Senior
Posted: April 24, 2025
On-site
EUR 75,000 - 95,000 annually based on Dublin market rates for senior validation roles in medical device sector

Benefits

Permanent position with stable employment
Professional development opportunities
Monday to Friday work schedule
Modern medical device manufacturing environment

Key Responsibilities

Lead technical validation team and manage APQP lifecycle
Drive regulatory compliance and validation strategy development
Oversee design transfer and equipment validation processes
Manage validation documentation and quality systems
Direct process improvement initiatives
Lead team of Validation Engineers

Requirements

Education

BSc / BEng or similar relevant technical degree

Experience

5 years high-volume engineering experience in medical device manufacturing, 3 years validation experience

Required Skills

Statistical techniques Minitab Six Sigma Process development Risk Analysis/Risk Management FMEA expertise Documentation skills Strong interpersonal and communication skills Process validation Technical problem-solving Team leadership

Certifications

Six Sigma Green Belt (preferred)
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Sauge AI Market Intelligence

Industry Trends

Medical device manufacturing is experiencing increased regulatory scrutiny, particularly in validation processes and documentation requirements Growing emphasis on digital transformation in validation processes, requiring expertise in electronic documentation systems Rising demand for validation engineers who can bridge quality assurance with operational efficiency

Role Significance

Typically leads a team of 3-7 validation engineers, interfacing with quality, operations, and engineering departments
Senior leadership position with significant influence on quality systems and regulatory compliance. Role combines technical expertise with team leadership and strategic planning.

Key Projects

New product validation implementation Process optimization and validation lifecycle management Regulatory compliance initiatives Quality system enhancement programs

Success Factors

Strong regulatory knowledge and ability to interpret GMP requirements Excellence in team leadership and cross-functional collaboration Advanced technical problem-solving capabilities Strategic thinking in validation planning and execution

Market Demand

High demand with sustained growth projected. Medical device manufacturing in Ireland continues to expand, with validation expertise being a critical skill set for regulatory compliance and operational excellence.

Important Skills

Critical Skills

Validation lifecycle management expertise - essential for ensuring regulatory compliance and product quality Statistical analysis and process control - crucial for scientific validation approach Risk management and FMEA expertise - fundamental to modern validation strategies

Beneficial Skills

Project management certification Advanced statistical software proficiency Quality system audit experience Industry 4.0 knowledge

Unique Aspects

Role combines validation expertise with strategic planning and team leadership
Position offers exposure to advanced medical device manufacturing processes
Opportunity to influence validation strategies at a system level

Career Growth

2-4 years in role before advancement opportunity, depending on project success and organizational growth

Potential Next Roles

Validation Manager Quality Systems Director Technical Operations Manager Regulatory Compliance Director

Company Overview

ICDS Recruitment Consultants

ICDS Recruitment Consultants specializes in technical and engineering placements for Ireland's growing medical device sector

Well-established recruitment firm serving major medical device manufacturers in Ireland
Strong presence in Dublin's medical device manufacturing hub
Professional consulting environment with focus on technical excellence and industry expertise
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