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Cég neve
HumanCentrum Kft.
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Munkavégzés helye
Prologis Üzleti Park - Gyál, Gorcsev Iván utca 7, 2360 -
Egyéb juttatások
- Mobiltelefon
- Cafeteria
- Szakmai tréningek
- Nyelvtanulás támogatása
- Munkába járás támogatás
- Egészségbiztosítás
- Élet- és balesetbiztosítás
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Munkaidő, foglalkoztatás jellege
- Teljes munkaidő
- Alkalmazotti jogviszony
- Általános munkarend
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Biztosított eszközök
- Laptop
- Desktop PC
- Headset
- Mobiltelefon
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Elvárások
- Angol felsőfok
- 3-5 év tapasztalat
- Egyetem
Kis türelmet...
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Állás leírása
HumanCentrum Kft.
Quality Validation Specialist
We are looking for a Validation Specialist on behalf of our international medical device manufacturing partner for a 1-year fixed term contract. The role supports the Quality Assurance team with validation and MDR-related activities.
Our partner is a globally recognized medical device manufacturer with decades of experience and a strong focus on innovation and high-quality production standards. The Hungarian site plays an important role in the company’s global quality engineering and manufacturing processes.
Our partner is a globally recognized medical device manufacturer with decades of experience and a strong focus on innovation and high-quality production standards. The Hungarian site plays an important role in the company’s global quality engineering and manufacturing processes.
Task:
- 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
Expectation:
- 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)
Other:
- Experience with MDR-related validation activities
- Knowledge of statistical monitoring systems
- Deeper hands-on experience in technical project environments
What we offer:
- 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
Sector(s):
- Manufacturing, Production
- Quality Assurance
- Engineer
- Quality Assurance Engineer
- Healthcare, Pharmaceutical Industry
- Quality Assurance
How to apply/ contact information:
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.
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