کارشناس تضمین کیفیت

پارس ایزوتوپ

منتشر شده 4 سال پیش

Job Description

- Supervising the production procedure and quality control of the radiopharmaceuticals - Inspecting the clean room based on GMP requirements - Inspecting and adhering to GMP requirements needed for the production line and labs - Preparing and reviewing the instructions of the related activities - Preparing the Batch Records and supervising their completion - Preparing the process validation and clean validation protocols and helping in their implementation - Cooperating in design, implementation and employing quality assurance systems - Carrying out internal audits - Preparing documentations - Editing, monitoring and analyzing process indexes - Recognizing and evaluating process risks and taking prevention measures

Requirements

- MSc. or PhD in Organic Chemistry, Analytical Chemistry, Applied Chemistry or Industrial Engineering or the related engineering - Having worked at any pharmaceutical companies or having the related experience for at least 3 years - Familiar with GMP requirements and pharmaceutical standards - A good command of English in all four skills - Familiar with Microsoft Office - Familiar with management system and product adaptation requirements - Familiar with recognition and documentation of processes - Holding an audit certificate related to quality management systems - Skilled in audit techniques and methods - Familiar with management system requirements at pharmaceutical industry - Preferably living in Tehran Personality: Accurate, disciplined, patient, hardworking, interested in teamwork

Employment Type

  • Full Time

Details

Employment type

  • Full Time

Educations

برای مشاهده‌ی شغل‌هایی که ارتباط بیشتری با حرفه‌ی شما دارد،