I am a dedicated Supplier Quality expert and certified Lead Auditor with a rich background in the Medical Device and GMP industry. Currently, I work at Thermo Fisher Scientific Baltics as a Staff Supplier Quality Engineer. My role involves evaluating and auditing supplier quality management systems, negotiating Supplier Quality Agreements, and resolving supplier-related quality issues. I am committed to ensuring compliance with ISO 9001, ISO 13485, GMP standards, and company SOPs, while also contributing to LEAN and Practical Process Improvements (PPI) projects.
With a Master’s degree in Biochemistry from Vilnius University and a Bachelor’s degree in Bioengineering from Vilnius Gediminas Technical University, I bring a strong technical foundation to my work. I thrive on managing projects, facilitating communication, and tracking overall project execution to ensure everything runs smoothly. My passion for continuous improvement and quality assurance drives me to excel in my field.
Searching for new customers
Managing sales projects and reports
Representing the company and handling promotional materials
Office administration and paperwork
Assisting the Office Manager with daily tasks
Preparing slide decks and arranging conferences for Medical Representatives
Monitoring daily reports
Preparing documents for new drug registration
Driving, leading, and facilitating meetings to consolidate progress updates
Managing risks and facilitating communication
Ensuring tracking of overall project execution
Ensuring project management compliance with ISO 9001, ISO 13485, GMP standards, and company SOPs
Following LEAN principles and actively participating in Practical Process Improvements (PPI) projects
Supplier QMS evaluation and auditing
Negotiating Supplier Quality Agreements (QAA)
Managing supplier-caused quality issues
Ensuring compliance with ISO 9001, ISO 13485, GMP standards, and company SOPs
Following LEAN principles and actively participating in Practical Process Improvements (PPI) projects
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