Hatice Sava
Angestellt, Field Office Administrator and Quality Responsible, Varian Medical Systems
İstanbul, Türkei
Über mich
Quality Professional with a total of 16+ years of experience with the experience of raw material quality control in the pharmaceutical industry, finished product quality analysis and R&D experience in the radiopharmaceutical industry, and quality system management experience in the medical device industry.
Werdegang
Berufserfahrung von Hatice Sava
Bis heute 3 Jahre und 11 Monate, seit Aug. 2020
Field Office Administrator and Quality Responsible
Varian Medical Systems
Represented the company in quality audits (ISO 9001) Managed the quality operations Created new SOPs Planned, performed, and reported internal audits of all departments Planned, performed, and reported Management Review Meetings Planned external audits Monitored the KPIs of all departments Identified and analyzed potential risks with department managers Trained all personnel regarding quality management program Managed the customer satisfaction surveys of all departments and managed customer complaints
8 Jahre und 3 Monate, Mai 2012 - Juli 2020
Quality Responsible & Operation Reporting Manager
Varinak Oncology Systems Sales and Services
Represented the company in quality audits (ISO 9001) Managed the quality operations Created new SOPs Planned, performed, and reported internal audits of all departments Planned, performed, and reported Management Review Meetings Planned external audits Monitored the KPIs of all departments Identified and analyzed potential risks with department managers Trained all personnel regarding quality management program Managed the customer satisfaction surveys of all departments and managed customer complaints
2 Jahre und 4 Monate, Jan. 2010 - Apr. 2012
Quality Control Specialist
Eczacıbaşı - Monrol Nuclear Products
Analyzed radiopharmaceutical products Followed up CAPAs and change controls with Quality Assurance Department Carried out R&D studies (Developing new analysis methods in HPLC and GC devices) Validated the product analysis methods used in laboratory Wrote validation protocols and reports Wrote stability protocols and reports Planned weekly workflow of the team (3 members)
4 Jahre und 1 Monat, Aug. 2005 - Aug. 2009
Quality Control Specialist
Abdi İbrahim Pharmaceuticals
Analyzed raw materials via using HPLC, GC, UV, AAS, Particle Counter, FTIR, etc. techniques and reported the test results Translated EP and USP Pharmacopeia analysis methods into Turkish and prepared SOPs Laboratory Training Responsible Gas Chromatography Devices Responsible MSDS Responsible
Ausbildung von Hatice Sava
1 Jahr und 10 Monate, Sep. 2011 - Juni 2013
Master of Science: Management in Pharmaceutical Industry
Acıbadem University
Sprachen
Türkisch
Muttersprache
Englisch
Fließend