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.