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1. Somayeh Raftari
LinkedIn: https://www.linkedin.com/?trk=nav_logo
Profile
I have a master degree in pharmacy and by working for more than 6 years at
quality department; I have a good knowledge and understanding of GMP
regulations and guidelines which have to be implemented in pharmaceutical
industries. My responsibilities included investigation of non-conformities and
planning for corrective actions. Involvement in qualification of pharmaceutical
instruments as well as quality control processes, reviewing change requests,
updating SOPs, supporting internal audits and some inspections were all parts of
my responsibilities in the quality department.
Work Experience
Razi Business
Development Co.
2012-2014
Quality Assurance Professional Address:
Vejlesøparken 1,1,-
118 2840 Holte ,
Copenhagen,
Denmark
Mobile: +45
91664593
Home: +45 48427173
Email:
dr.raftari@yahoo.com
Date of birth:
16th, Sep.80
 Order and purchasing of pharmaceutical products;
 Maintaining stock, handling and storing products
properly;
 Involvement in preparing and reviewing SOP;
 Preparing training courses in compliance with GMP
regulations and participation in different internal
audits;
 Implementation of GDP and GSP at company’s
warehouses;
 Non-conformity investigation and planning for
corrective actions;
Sina Darou
Pharmaceutical
Company
2010-2012
Quality Assurance Professional IT Skills:
MS office including
Word, Excel,
PowerPoint
Advanced use of
internet
Language Skills:
Persian: Native
English: Professional
proficiency
Danish: Intensive
course, module 4
 Involvement in preparing and reviewing SOP;
 Involvement in review and approval of batch records
and related documents;
 Investigation of non-conformity and planning for
corrective actions;
 Qualification of analytical equipment;
 Preparing training courses for technicians and
operators;
 Participating in regular monthly and yearly internal
audits.
Chemi Darou
Pharmaceutical

2. Company
2008-2010
Qualified Pharmacist in Quality Department Personality:
self-driven
ambitious
good at multi-tasking
fit into a group easily
as an individual
 Responsible for quality tasks such as: preparing and
reviewing SOP, review and approval of batch records
and related documents, non-conformity investigation
making plan for corrective actions;
 Assessment of raw material qualification to be in
compliance with GMP and internal regulations;
 Preparing training courses in compliance with GMP
regulations;
 Regular monthly and yearly internal audits
 Evaluation of contracts with suppliers to be in
compliance with internal, external rules and regulatory
affair regulations.
Shahid Andarzgou
Hospital Pharmacy
(Bazarganan)
2004-2008
Technical Supervisor
 Dispensing prescription medicines to the public;
 Checking dosage and ensuring that medicines are
correctly and safely supplied and labelled;
 Supervising the preparation of any medicines;
 Liaising with doctors about prescriptions;
 Selling over-the-counter medicines;
 Advising patients of any adverse side-effects of
medicines or potential interactions with other
medicines/treatments;
 Managing, supervising and training pharmacy support
staff
Education
Cand. Pharm. Mashhad University of Medical Sciences,
Faculty of pharmacy
Relevant Courses
 Fundamentals of Good Manufacturing Practice (GMP);
 Calibration, PSH, Tehran, Iran, 2008.
Interests
Reading books, Shopping, Movie, Music, Dance, Crazy
about doing every exciting things such as Skydiving,
Climbing, Scuba diving.
References: Available on request