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Validation Engineer I - Job Opportunity at Thermo Fisher Scientific

Hoogkerk, Netherlands
Full-time
Entry-level
Posted: May 18, 2025
On-site
EUR 45,000 - 55,000 annually based on entry-level position in Netherlands biotech sector

Benefits

GMP-compliant work environment
PPE provided
Professional development opportunities
Technical training programs

Key Responsibilities

Lead validation and qualification processes for GxP systems
Coordinate process validation studies and documentation
Provide technical expertise for manufacturing activities
Ensure compliance with regulatory standards
Support continuous improvement initiatives
Manage validation master plan execution

Requirements

Education

Higher vocational education, BSc or equivalent in Validation, Engineering, or Chemical Technology

Experience

Proven experience in Validation or Technical role in Biotech/Biopharma/cGMP environment

Required Skills

Clear communication Data-driven problem solving Planning and organization Self-awareness Good command of English Knowledge of EH&S Knowledge of biologics manufacturing facilities
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Industry Trends

Increasing focus on biologics manufacturing driving demand for validation expertise Growing regulatory complexity in GMP environments requiring specialized validation knowledge Digital transformation in pharma manufacturing creating need for computer system validation skills

Role Significance

Typically part of a 5-8 person validation team within larger quality organization
Entry-level position with potential for significant impact on quality and compliance outcomes

Key Projects

Equipment and process validation implementation Computer system qualification Utility system validation Documentation system maintenance

Success Factors

Strong understanding of GMP requirements and validation principles Ability to collaborate across multiple departments Detail-oriented documentation skills Proactive problem-solving approach

Market Demand

High demand due to expanding biologics manufacturing sector and increasing regulatory requirements

Important Skills

Critical Skills

GMP knowledge - essential for ensuring regulatory compliance Technical documentation - crucial for validation activities Cross-functional communication - key for project success

Beneficial Skills

Project management skills Statistical analysis capabilities Automation system knowledge

Unique Aspects

Focus on biologics manufacturing validation provides specialized experience
Opportunity to work with cutting-edge bioprocessing technologies
Strong emphasis on GMP compliance and quality systems

Career Growth

2-3 years to Senior Validation Engineer, 4-5 years to team lead positions

Potential Next Roles

Senior Validation Engineer Validation Team Lead Quality Systems Manager Technical Operations Manager

Company Overview

Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, with significant presence in analytical instruments, equipment, consumables and software for research, analysis, discovery and diagnostics

Fortune 500 company with strong market position in life sciences and laboratory products
Strategic location in Netherlands biotech hub with significant European operations
Professional environment with emphasis on scientific excellence and regulatory compliance
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