Neringa Kaminskienė

Quality Control Officer, Researcher at KELI Therapeutics
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Contact Information
us****@****om
(386) 825-5501
Location
Kaunas, Kauno, Lithuania, LT

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Experience

    • Lithuania
    • Biotechnology Research
    • 1 - 100 Employee
    • Quality Control Officer, Researcher
      • Mar 2020 - Present

      Played a pivotal role in developing and implementing quality control and assurance strategies and procedures for ATMP manufacturing, ensuring compliance with GMP and other regulatory guidelines. Played a pivotal role in developing and implementing quality control and assurance strategies and procedures for ATMP manufacturing, ensuring compliance with GMP and other regulatory guidelines.

    • Lithuania
    • Higher Education
    • 400 - 500 Employee
    • Junior Researcher
      • Dec 2021 - Sep 2023

      Project "Development of an innovative cellular therapy prototype for the treatment of acute respiratory failure syndrome caused by the SARS-COV-2 virus" Project "Development of an innovative cellular therapy prototype for the treatment of acute respiratory failure syndrome caused by the SARS-COV-2 virus"

    • Lithuania
    • Civil Engineering
    • 1 - 100 Employee
    • Pharmacist
      • Sep 2021 - Sep 2022

      In my role, I provide consultation services to clients regarding the implementation of GMP licenses in accordance with EU and Lithuanian laws and regulations. I also clarify advanced therapy requirements based on existing laws in these regions and assist with the preparation of documents for GMP activities applications. Additionally, I facilitate the implementation of GMP licenses and advanced therapy treatment activities within customer accounts. In my role, I provide consultation services to clients regarding the implementation of GMP licenses in accordance with EU and Lithuanian laws and regulations. I also clarify advanced therapy requirements based on existing laws in these regions and assist with the preparation of documents for GMP activities applications. Additionally, I facilitate the implementation of GMP licenses and advanced therapy treatment activities within customer accounts.

    • Latvia
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Pharmacist
      • Sep 2019 - Jul 2022

    • Lithuania
    • Hospitals and Health Care
    • 300 - 400 Employee
    • Pharmacist
      • Sep 2016 - Sep 2018

      Oncology pharmacist. Developed and implemented quality control procedures for centralized cytotoxic drugs preparation in the hospital pharmacy's cleanroom, ensuring compliance with regulatory guidelines and patient safety standards. Collaborated with the pharmacy team to establish and improve standard operating procedures (SOPs) for the safe handling, preparation, and disposal of cytotoxic drugs, ensuring adherence to best practices and regulatory requirements. Assisted in the design and implementation of a comprehensive quality management system (QMS) specifically tailored for cytotoxic drugs preparation, focusing on risk assessment, monitoring, and continuous improvement. Conducted internal audits and self-assessments to identify areas for improvement, document findings, and recommend corrective actions to enhance the quality and safety of cytotoxic drugs preparation processes. Collaborated with healthcare professionals, including pharmacists, nurses, and physicians, to provide training and education on safe handling practices and proper use of personal protective equipment (PPE) in the cleanroom environment. Show less

    • Lithuania
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Pharmacist
      • 2013 - Sep 2016

Education

  • Lithuanian University of Health Sciences
    Master's degree, Pharmacy
    2008 - 2013

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