QA Document Reviewer
Our client a major pharmaceutical company are currently looking for a QA Document Reviewer to work in their busy production department. This is a permanent job opportunity that comes with a whole host of benefits.
The main purpose of the job role will be to organise and control the documentation flow within the department
Documentation will be done in a timely manner so that the processing of the sterile product is commenced in accordance with the planned operational requirements and GMP
Reviewing all bulk product documentation for compliance and regulations purposes and providing feedback to the operational team
To generate and review all departmental documentation and update all necessary departments
Communicate with other departments within the organisation
What We need
The nature of the role requires someone with either a Degree qualification (or equivalent) in a technical/scientific discipline is desirable. Someone with an engineering, quality or production environment is a must. If you have knowledge of the processes associated with sterile products production would be great!
To get the ball rolling, please press the apply now button on this screen.
Job Reference: JOB-4305