شرایط احراز:
• PhD in Pharmacy
• Professional work experience in the pharmaceutical industry and production for at least 3 years.
• Proficient in regulatory matters and contract manufacturing.
• Proficient in quality assurance standards and laws. Has experience in implementing pharmaceutical regulations and laws and related monitoring.
• Proficient in standards and documentation.
• Ability to communicate continuously with regulatory bodies. with drugs and supplements.
• Familiar with the procedures of obtaining, renewing and amending permits and licenses related to raw materials and drug and supplement product production. and the TTAC system.
• Familiar with matters related to the follow-up, registration and clinical trials related to the product.
• Has experience working with the drug and supplement department. Factory.
• Familiarity with GMP and GLP standards.
• Ability to work in a team environment.
• Ability to analyze and solve problems.
• Strong communication skills.
• Fluent in English. .
• Familiarity with office software (PowerPoint, Excel, Word, etc.)
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