Quality Validation Specialist

• Execution of validation and testing activities according to quality requirements
• Validation and qualification of manufacturing and testing equipment
• Supporting the preparation of validation protocols, reports, and maintenance procedures
• Identifying and documenting potential process or equipment gaps
• Performing validation tasks to support manufacturing technologies and products
• Conducting installation, operational, and performance qualification studies
• Ensuring critical operating parameters remain within qualified limits
• Implementing equipment enhancements in line with quality expectations
• Documenting deviations and investigations related to MDR remediation tasks

• Experience in quality validations within a manufacturing environment, preferably medical device
• Proficiency in validation testing and statistical process control/monitoring
• Understanding of medical device standards and regulations
• Ability to prepare technical documentation and reports
• Strong statistical and mathematical skills
• Solid problem-solving abilities and systems thinking
• Intermediate level knowledge of Excel, Word, and PowerPoint (advanced is an advantage)

• Monday to Friday, regular daytime schedule

• Stable, international company background
• Competitive compensation package
• Professional development opportunities in a global environment
• Exposure to modern manufacturing and engineering technologies
• Supportive and experienced professional team

• Experience with MDR-related validation activities
• Knowledge of statistical monitoring systems
• Deeper hands-on experience in technical project environments

If you are interested in this opportunity, please submit your CV through the application platform. Our recruitment team at Humán Centrum will contact shortlisted candidates and support you throughout the entire selection process on behalf of our partner company.