Senior Validation Engineer - Job Opportunity at ICDS Recruitment Consultants

Dublin, Ireland
Full-time
Senior
Posted: March 26, 2025
On-site
EUR 75,000 - 95,000 per year based on Dublin market rates for senior validation engineering roles in medical devices

Benefits

Permanent position offering job security
Professional development opportunities in validation engineering
Technical leadership role with team management responsibilities

Key Responsibilities

Lead validation team and manage technical/equipment validation projects according to regulatory standards and protocols
Drive design transfer process and oversee APQP lifecycle implementation
Develop and maintain validation strategies compliant with regulatory requirements and GMP standards
Manage team of validation engineers including work allocation, performance review, and professional development
Create and control PFMEA and validation documentation throughout product lifecycle

Requirements

Education

BSc / BEng or similar relevant technical degree

Experience

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

Required Skills

Statistical techniques expertise Minitab proficiency Six Sigma knowledge Process development experience Risk Analysis/Risk Management FMEA expertise Strong documentation skills Strong interpersonal and communication skills Process validation expertise Technical problem-solving capabilities

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 Integration of digital validation tools and automated documentation systems is becoming standard practice Growing emphasis on risk-based validation approaches aligned with FDA and EU MDR requirements

Role Significance

Typically manages 3-5 validation engineers in medical device manufacturing environment
Senior leadership position with direct influence on product quality and regulatory compliance. Role involves both technical expertise and team management responsibilities.

Key Projects

New product validation implementations Process optimization and validation programs Regulatory compliance initiatives Quality system improvements

Success Factors

Strong technical background combined with leadership capabilities Deep understanding of medical device regulatory requirements Ability to balance technical accuracy with project timelines Excellent stakeholder management skills across multiple departments

Market Demand

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

Important Skills

Critical Skills

Validation lifecycle management in medical devices Statistical analysis and process validation Risk management and FMEA expertise Team leadership and project management

Beneficial Skills

Six Sigma methodologies Automated validation tools Change management expertise Quality system optimization

Unique Aspects

Role combines technical validation expertise with team leadership
Position at intersection of quality, engineering, and regulatory compliance
Opportunity to influence validation strategies at organizational level

Career Growth

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

Potential Next Roles

Validation Manager Quality Director Technical Operations Manager Manufacturing Engineering Manager

Company Overview

ICDS Recruitment Consultants

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

Established recruitment firm serving major medical device manufacturers in Ireland
Strong presence in Dublin's medical device manufacturing hub
Professional environment focused on technical excellence and regulatory compliance
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