مهر گستر تامین دارو

بیش از یک ماه منتشر شده

سمت شغلی

شرکت

حقوق

آمار رزومه‌های ارسال شده

Job Description

• Good knowledge about writing SOP, SMF, VMP, different validation protocols and other related documents • Familiar with international GMP guidelines specially PIC/S • Familiar with Pharmacopeia especially USPE • Establishment of strong QA system in OSD manufacturing site. • Validation and Qualification Management • Coordinating inspection and audit arrangements • Providing support in all areas of quality • Identifying opportunities for improvement of quality processes • Administering quality activities • Identifying opportunities for improvement of regulatory processes

Requirements

• The ideal candidate will be an Pharm.D or MSc in Medical Sciences • Minimum 4 year previous experience in Pharmaceutical Quality systems (You have worked in a quality or production department) • Should be able to demonstrate the ability to work on your own initiative • Good IT skills • Good understanding of the relevant PIC\S , EU guidelines and Iranian and regulatory framework is required • Good communication skills • Time management and high attention to detail and accuracy • Fluent in English

Employment Type