• Project Development: Involved in initiation of biotherapeutic drug development project.• Grant Application: Involved in preparation of grant proposals related with biotherapeutics.• Data Analysis and Visualization: Proficiently utilized advanced formulas and macros in Excel to create automated documents for data analysis and visualization purposes.• Web Development and SEO Implementation: Designed multiple websites using WordPress while implementing SEO best practices for enhanced online visibility.• SEO-Centric Content Development: Creation of SEO-Optimized and Reader-Friendly Website Content• Graphic Design Proficiency: Crafting brochures, banners, and more utilizing Adobe programs and Canva

I am involved in different projects at Nobel Pharmaceuticals, which include COVID vaccine development and production, biosimilar development, grant applications, GMP/GLP processes.• Developed, validated, and prepared over 25 methods (in both Turkish and English) for six distinct molecules, utilizing various instruments such as HPLC, CE, LC-MS, and plate reader, demonstrating a strong command over analytical technique.• Proficiently analyzed data using Excel and other tools for both preclinical and clinical applications, extracting valuable insights and supporting evidence-based decision-making.• Produced technical documents and industry-specific materials, including Standard Operating Procedures (SOPs), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Instruction manuals, and CSV documents, showcasing meticulous attention to detail and compliance with regulatory standards.• Ensured the accuracy and reliability of analysis results and documentation by collaborating closely with Quality Assurance and Quality Control teams, exemplifying a commitment to maintaining high-quality standards.• Engaged in fruitful collaborations to prepare and present more than seven grant applications, while also leading the effort in four grant applications, reflecting strong teamwork and leadership skills in achieving successful outcomes.

promoted to Bioprocess Specialist position.

Started to work as Bioprocess engineer

– Managed timely start-up, documentation, and monitoring of clinical trials onsite.– Coordinated with research teams to meet recruitment targets and timelines.– Built relationships with key stakeholders, including research leads, PIs, center staff, and sponsors.– Worked with patients during all trial assessments and treatments.– Prepared for and hosted monitoring and close-out visits.– Ensured compliance with SOPs, GCP guidelines, and regulatory requirements.

Development of SPR device and kitsGathered, arranged and corrected research data to create representative graphs and charts highlighting results for presentations.Identified sources of funding to prepare research proposals and submit funding applications.Interpreted data analysis results to draw inferences and conclusions.Sorted data into well-organized formats and transformed into figures.Performed research into study topics to increase knowledge and to provide valuable contributions.

Involved in signalling pathway related projectCollaborated with leadership team to identify relevant questions and determine best methods of collection.Determined areas of research to increase knowledge in particular field.

Development of contrast agent for MRIGathered, arranged and corrected research data to create representative graphs and charts highlighting results for presentations.Planned, modified and executed research techniques, procedures and tests.Used various types of lab equipment related with Nanobiology.Prepared materials for reports, presentations and submission to peer-reviewed journal publications.