Job Responsibilities:
- Coordinate the reception of change control request and determine the areas involved for further evaluation by each of them.
- Establish a defined change control process to approve or reject the change and involves appropriate stakeholders.
- Compile the activities to be performed by involved stakeholders after integration and reevaluation of all the proposed actions indicated by the responsible in the involved area/s. The final list of activities is revised to align the sequence of actions according to the timeline.
- Follow up on Change tasks performed to ensure actions are properly implemented within defined target date.
- Review data submitted by stalk holders needed to complete tasks or change control authorization.
- Follow up on post implementation actions and post verification actions for Change control closure.
Professional Experience Required:
- Typically requires a minimum of 2 years of related experience, within GMP background in a
- Pharmaceutical industry.
- Bachelor s Degree in Health-related Sciences.
- Knowledge of Quality Management.
- Knowledge of cGMP requirements preferred.
- Written and spoken English and Arabic.
