Gunay Kizil
Gunay Kizil has over 15 years of experience in the pharmaceutical industry, particularly in manufacturing, process review, and quality assurance. Trained in software testing, with skills in technical problem-solving and documentation in GMP environments.
AI analysis: Personality & work environments
The content in this CV is automatically created by SuperRen after an AI conversation, where Gunay Kizil shared his experiences, skills and personal strengths.
Work environments
Gunay has extensive experience in GMP-regulated pharmaceutical manufacturing environments, indicating a high level of familiarity with regulatory compliance and quality assurance processes.
As a person
Demonstrates a strong inclination towards structured problem-solving and continuous improvement, indicating a proactive and detail-oriented individual.
Previous experience
Procell
Manufacturing Engineer
2023-2025
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Manufacturing of stem cell therapies, preparation of GMP-critical documentation, participation in projects, and management of CAPAs.
This role indicates a commitment to advanced manufacturing processes and proactive engagement in continuous improvement, highlighting leadership in compliance.
Octapharma AB
Process Reviewer
2020-2023
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Review batch documentation for compliance, manage deviations, and coordinate production orders.
Reinforces expertise in regulatory compliance and highlights analytical skills in ensuring quality.
Octapharma AB
Document Coordinator
2019-2020
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Responsible for documenting in GMP compliance, handling deviations, and supporting teams with document improvements.
Demonstrates strong administrative and coordination skills, essential for ensuring quality in pharmaceutical processes.
Octapharma
Aseptic Technician
2012-2019
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Worked in drug production processes, ensuring quality through various technical tasks and validations.
Foundation role that provided practical experience and skills in pharmaceutical manufacturing, contributing to a deeply technical background.