Job Description

  • Monitoring the implementation of product production rules based on the GMP standard and the requirements of regulatory organizations.
  • Participation in the evaluation of suppliers based on GXP principles, control with criteria and standards.
  • Supervising how to conduct tests and ensure the provision of quality products.
  • Ensuring compliance with the principles of GXP through monitoring the implementation of cleaning equipment and production spaces, the process of eliminating pharmaceutical and non-pharmaceutical waste, etc., in order to comply with the principles and standards of GXP.
  • Supervising the preparation and presentation of necessary files and documents for pharmaceutical, herbal, supplement, pharmaceutical products, etc.
  • Ensuring the correct implementation of the processes of supply, handling, storage, and control of materials and manufactured products.
  • Establishing effective communication with regulatory organizations by attending meetings and making necessary inquiries in order to speed up and facilitate the current affairs of the company.

Requirements:

  • Proficient in GXP principles, pharmacopoeias and pharmaceutical standards.
  • Proficient in documentation and report writing.
  • Ability to solve problems and make decisions.
  • Flexibility.
  • Effective communication skills.
  • Thorough knowledge of GMP and TTAC.

Employment Type

  • Part Time

Details

Employment type

  • Part Time

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