شرایط احراز:
Proficient in quality assurance standards and laws.
Experience in implementing pharmaceutical regulations and laws and related monitoring.
Proficient in standards and documentation.
Ability to communicate continuously with regulatory bodies. Product registration documents and the ability to prepare documents related to drugs and supplements.
Familiar with the procedures of obtaining, renewing and amending permits and licenses related to raw materials and the production of drug and supplement products.
Familiar with the registration systems of the Food and Drug Organization and Product registration procedures in Chargoon and TTAC system.
Proficient in preparing quality documentation for export. and supplements.
Ability to be stationed at the factory at least 3 days a week.
A degree in pharmacy.
Professional work experience in the pharmaceutical industry.
Familiarity with GMP standards and GLP.
Ability to work in a team environment.
Ability to analyze and solve problems.
Strong communication skills. Pharmaceutical
Mastery of the basics and methods of inventory control of items in the warehouse
Mastery of the knowledge of pharmaceutical raw materials
Familiarity with warehouse software
Familiarity with the calibration methods of devices and Equipment
Familiarization with the principles and basics of planning production and materials
این آگهی از وبسایت ایران تلنت پیدا شده، با زدن دکمهی تماس با کارفرما، به وبسایت ایران تلنت برین و از اونجا برای این شغل اقدام کنین.