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QA Validation Specialist - Job Opportunity at QA Resources

Cork, Ireland
Contract
Mid-level
Posted: January 20, 2025
On-site
EUR 45,000 - 65,000 per year based on Cork market conditions and pharmaceutical industry standards

Benefits

Project-based contract work offering professional development opportunities
Exposure to cutting-edge pharmaceutical validation processes
Collaborative work environment with industry leaders

Key Responsibilities

Lead validation protocol development and review for critical pharmaceutical systems and processes
Manage and execute site Validation Master Plan with strategic oversight
Serve as primary vendor liaison for qualification activities and documentation
Drive cGMP compliance through documentation authorship and quality oversight
Provide expert QA support for equipment qualification processes

Requirements

Education

Bachelor's Degree in scientific or engineering discipline

Experience

Minimum of 2+ years in pharmaceutical industry

Required Skills

cGMP knowledge Validation protocol development Documentation authorship Equipment qualification Verbal and written communication Interpersonal skills Organizational skills Software validation Process validation Cleaning validation Equipment validation Facilities validation Utilities validation
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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 risk-based validation approaches aligned with FDA and EMA guidelines Rising demand for validation specialists with combined QA and technical expertise

Role Significance

Typically part of a 5-10 person validation team within larger quality organization
Mid-level specialist role with significant responsibility for quality system integrity and compliance assurance

Key Projects

Major equipment qualification initiatives Facility validation programs Software system implementations Process validation campaigns Regulatory compliance projects

Success Factors

Strong technical writing abilities combined with analytical thinking Excellent understanding of regulatory requirements and their practical application Ability to manage multiple validation projects simultaneously while maintaining quality standards Strong vendor management and stakeholder communication skills

Market Demand

High demand driven by expanding pharmaceutical manufacturing presence in Ireland and increased regulatory requirements

Important Skills

Critical Skills

Validation protocol development - Essential for ensuring compliance and product quality cGMP knowledge - Fundamental to all quality activities in pharmaceutical manufacturing Technical writing - Critical for documentation and compliance requirements

Beneficial Skills

Project management capabilities Risk assessment methodology Data integrity principles Quality management systems knowledge

Unique Aspects

Role combines technical validation expertise with quality system oversight
Position offers exposure to multiple pharmaceutical systems and processes
Opportunity to work in Ireland's growing pharmaceutical sector

Career Growth

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

Potential Next Roles

Senior Validation Specialist Validation Manager Quality Systems Manager Compliance Manager Technical Operations Manager

Company Overview

QA Resources

QA Resources is a specialized pharmaceutical industry staffing and consulting firm focusing on quality assurance and validation services

Established presence in Ireland's pharmaceutical sector with connections to major manufacturers
Strong positioning in Cork's pharmaceutical hub with access to multiple client sites
Project-based environment with emphasis on technical expertise and professional development
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