Lead QA Technician - Job Opportunity at Thermo Fisher Scientific

Bleiswijk, Netherlands
Full-time
Mid-level
Posted: May 6, 2025
On-site
EUR 45,000 - 60,000 annually based on location and role requirements

Benefits

GMP-compliant work environment
Professional development opportunities
Role in critical pharmaceutical quality assurance
Industry-leading laboratory facilities

Key Responsibilities

SOP Management and Document Control coordination
Quality review and approval of Trackwise QRs
Product/material status control management
Supplier assessment execution
Quality Management System compliance oversight
EU GMP and IGJ regulatory compliance assurance
Archival duties management
Quality verification execution
Training and proficiency assessment provision
Documentation review and approval
QC function execution

Requirements

Education

Degree level in relevant subjects

Experience

1 year GMP experience minimum

Required Skills

High degree of accuracy and attention to detail Procedure and regulation interpretation Problem solving Presentation and communication skills Mathematical calculation abilities MS Office proficiency Team collaboration Pressure management English language proficiency
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Sauge AI Market Intelligence

Industry Trends

The pharmaceutical QA sector is experiencing increased regulatory scrutiny, particularly in EU markets, driving demand for GMP-experienced professionals Digital transformation in quality management systems is creating need for technical expertise combined with traditional QA skills Growing focus on supply chain integrity is elevating the importance of supplier assessment capabilities

Role Significance

Typically operates within a QA team of 5-10 professionals in similar facility sizes
Mid-level leadership position with significant operational impact and quality oversight responsibilities

Key Projects

Quality Management System optimization initiatives Regulatory compliance programs Supplier qualification projects Documentation system improvements Team training and development programs

Success Factors

Strong understanding of EU GMP and IGJ regulations Ability to balance multiple quality system priorities Excellence in documentation practices Effective stakeholder management across departments Technical proficiency with quality management systems

Market Demand

High demand, particularly in European pharmaceutical manufacturing hubs

Important Skills

Critical Skills

GMP compliance expertise essential for maintaining regulatory standards Documentation management skills crucial for quality system integrity Technical understanding of quality management systems necessary for daily operations

Beneficial Skills

Project management capabilities Risk assessment experience Quality metrics analysis skills Regulatory audit experience

Unique Aspects

Specialized cleanroom environment requirements
Critical role in maintaining pharmaceutical quality standards
Combined QA/QC responsibilities
International regulatory compliance focus

Career Growth

2-4 years in role typically required before advancement to management positions

Potential Next Roles

Quality Assurance Manager Regulatory Compliance Manager Quality Systems Director Validation Manager

Company Overview

Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, with significant presence in laboratory products and services

Fortune 500 company with strong market position in analytical instruments and laboratory supplies
Strategic European location supporting critical quality operations
Professional environment with strong focus on compliance and quality excellence
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