Humán Centrum

Feladatok

• 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;

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

• 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

• Pest megye