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Quality System Analyst

 

The company

Our client is the international leader in the pharmaceutical arena, with the prominent role of finding the cure to one of the most spread illnesses - cancer. The company aims to find and implement a different and more effective way of cancer treatment.

 

The role

As a Quality Systems Analyst, you will be responsible for ensuring the documentation processes are in line with the GMP regulations, as well as, working closely with the change control systems and CAPA systems. Furthermore, you will provide additional guidance for the compliance regulations.

 

Responsibilities

-Ensuring that Deviation and CAPA management systems work correctly, also you will report the results to the Deviation Board.

-Monitoring the administrative part of the process and ensuring all the documentation is in line with the cGMP documents.

-Work with the Change Control and Quality Control systems to maintain the quality policies in a manufacturing facility.

 

Requirements

-Experience and knowledge in GMPs and pharmaceutical industries.

-Working experience with CAPA, Change Control, Audits, and other quality systems.

-Knowledge and experience in manufacturing processes.

-Strong written and oral communication in English. 

 

Other information

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