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Quality Control Systems Specialist - Job Opportunity at AstraZeneca

Dublin, Ireland
Full-time
Mid-level
Posted: January 21, 2025
On-site
EUR 55,000 - 75,000 per year based on Dublin market rates for specialist QC roles in pharmaceuticals

Benefits

Competitive bonus structure indicating performance-based compensation
Professional development opportunities through cross-functional exposure
Global pharmaceutical company benefits package
Modern quality systems technology exposure

Key Responsibilities

Lead master data management across multiple quality control systems (SAP, GQCLIMS, eLab, etc.)
Coordinate and execute quality documentation approvals ensuring GMP compliance
Provide first-line technical support and training for QC systems
Support cross-functional improvement initiatives and technical evaluations
Manage quality control aspects of internal/external audits
Drive analytical technology transfer processes

Requirements

Education

Degree in scientific discipline (preferred)

Experience

Experience working in GMP environment

Required Skills

GMP environment experience Quality assurance understanding IT systems knowledge (SAP, GQCLIMS, eLab, 1Lab, Empower, EM, MODA, WebCoA, CIMS, eWM) Strong attention to detail Good communication skills Cultural awareness Financial governance awareness Project management capabilities Technical evaluation expertise Documentation management skills
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Sauge AI Market Intelligence

Industry Trends

Pharmaceutical quality control is experiencing rapid digitalization with integration of multiple specialized systems requiring expertise in data management and system validation Increasing regulatory scrutiny in pharmaceutical manufacturing is driving demand for specialists who can manage complex quality systems Growing emphasis on data integrity and electronic systems validation in pharmaceutical quality control

Role Significance

Typically part of a 10-15 person quality control team in a larger quality organization of 50-100 people
Mid-level specialist role with significant system ownership responsibilities and cross-functional influence

Key Projects

Quality systems integration and optimization initiatives Regulatory compliance improvement projects Technical transfer programs for new product introductions System validation and upgrade implementations

Success Factors

Deep understanding of GMP requirements and quality systems integration Strong technical aptitude with ability to manage multiple complex systems Excellence in cross-functional communication and stakeholder management Proactive problem-solving approach with strong attention to detail

Market Demand

High demand driven by pharmaceutical industry expansion in Ireland and increasing complexity of quality systems

Important Skills

Critical Skills

GMP compliance expertise - fundamental for maintaining regulatory standards Technical systems knowledge - essential for managing multiple quality platforms Communication skills - crucial for cross-functional effectiveness

Beneficial Skills

Project management capabilities Change management experience Statistical analysis knowledge Lean manufacturing understanding

Unique Aspects

Exposure to multiple advanced quality control systems
Cross-functional involvement in technical transfers and system improvements
Balance of technical expertise with business process understanding

Career Growth

2-4 years in role before advancement, depending on project success and leadership demonstration

Potential Next Roles

Senior Quality Systems Specialist Quality Control Manager Quality Systems Manager Validation Manager

Company Overview

AstraZeneca

AstraZeneca is a leading global biopharmaceutical company with strong presence in oncology, respiratory, and cardiovascular therapeutics

Top-tier pharmaceutical company with significant market share and robust R&D pipeline
Strategic importance of Dublin location as part of European operations network
Innovation-focused environment with emphasis on scientific excellence and quality standards
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  • Critical success factors and key skills
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