Quality Assurance Control
Resume:
Sara Kafan
Cell: 919-***-****
E-Mail: *************@*****.***
Professional summery
Chemist, Master of Science in Inorganic chemistry, with over 5 years of experience in pharmaceutical companies. After training, began my career as "in process control" director with responsibilities in the areas of inspecting units, training personnel, manufacturing process control. After three years, was promoted to Director of Documentation in quality assurance position. Also issued standard operation procedure for production process and QA units according to PIC and GMP along with training quality assurance control and documentation standards to the personnel of the department.
Skills
Proficient in quality assurance.
Proficient in IPQC tests and control.
Proficient in Microsoft Office (Excel, Word and PowerPoint).
Experienced with pharmaceutical documentation (SOP, CAPA, Change Control, batch sheet master formula)
Proficient in quality control process and quality assurance
Possess ability to build relationship with co-workers, suppliers and clients
Competent in pharmaceutical standards (GMP, PIC/S, ISO)
Competent in Quality Control of raw materials, semi-finish and finished products
Competent with institutional pharmacy
Competent with analytical instruments for measuring specs (GC, dissolution,pH-meter, UV-VIS)
Work History
December 2015 - February 2017
NOVARTIS (MODAVA pharmaceutical co) IRAN-Alborz
Director of documentation in quality Assurance
Issued standard operation procedure (SOP) for quality assurance units according to PIC/s and GMP
Issued standard operation procedure (SOP) for production unit according to PIC/s and GMP
Trained quality assurance standard to personnel of factory
Inspected pharmaceutical units periodically
Controlled conformation of process with quality standard
Competent in validation process
May 2015 - December 2015
Novartis (Modava pharmaceutical Co) Iran
Expert of Quality Assurance
Competent in control and distribution of documents
Competent in inspection of production and storage process
Competent in documents control according to PIC/s, GMP, and USP.
January 2016 - March 2016
SOHA Pharmaceutical co. Iran
Expert of Quality Control
Expert in Quality Control of raw materials, semi-finish and finished products
Tested raw materials, checked production process and sampled finished products according to USP
Collected data and created quality control reports for management
Expert in analytical test (content,assay.dissolution, disintegration)
Competent with use of analytical instrument (pH-meter, Dissolution,, UV.Visible, Karl Fischer, IR )
Expert in Quality control of water in pharmaceutical company
April 2012 - December 2014
SOHA pharmaceutical Co. Iran
Director of IPQC unit
Competent in management of personnel and process
Proficient in control of production process of tablets and capsules
Proficient in control of cleaning and clearance production line
Competent in collection and analysis of data
Competent in personnel training
February 2012 - April 2012
SOHA pharmaceutical co. Iran
Expert of IPQC
Proficient in "In process control" of production process
Proficient in IPQC tests (weight, moisture, disintegration time, hardness,dimension)
Competent in works with IPQC instruments(disintegration tester, moisture balance, hardness tester)
Competent in sampling of raw materials, semi-finish and finished products
Education
2011 Zanjan University Iran-Zanjan,
Master of Science in Inorganic chemistry
Thesis: Zeolite-encapsulate iron hedrazon complex as an active catalyst for alkenes oxidations
2009 Zanjan University Iran-Zanjan,
Bachelor of Science in chemistry
Certifications
GMP(Good Manufacturing Practice) certification
GDP (Good Documentation Practice) certification
GLP (Good Laboratory Practice) certification
ICDL (international computer driving license) certification
" In process control in pharmaceutical industry" certification
"Quality Assurance in pharmaceutical industry" certification
"General Calibration in pharmaceutical industry" certification
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