Supervise, coordinate and direct all activities related to the operation and continuous improvement of the Quality Management System and Regulatory affair.As QA Manager:

• Responsible for the development, implementation and improvement of the Quality Management System.
• Supervise the implementation of the Quality Management System in all departments of the Company, monitors its operation and reports to the Management suggesting improvements.
• Represent the Company in its relations with third parties, e.g. customers, consultants, certification bodies, etc., in quality related matters.
• Supervise and coordinate the implementation of corrective and preventive actions.
• Supervise and coordinate the recording and evaluation of customer complaints.
• Supervise and coordinate the measurement of customer satisfaction.
• Is responsible for document control (quality system documentation).
• Has responsibility for ensuring that customer requirements are known and understood through-out the company.
• Has responsibility for ensuring that processes are in place to meet customer confidentiality requirements throughout the company.
• Represent the company\'s management on quality matters.
• Is responsible for the immediate transfer to the appropriate department (pharmacovigilance), of any adverse event information related to the Company\'s formulations.
• Is responsible for the immediate transfer to the appropriate department (medical information), of any medical information relating to the Company\'s formulations..

Opportunity to join a leading organization.|Organization with potential of expanding in the middle east region.

• Bachelor Degree in Sciences/ Pharmaceutical
• 5 year experience in the Company\'s Pharmaceuticals in Quality As QP Role

• European speciality pharmaceutical company.

Explore an opportunity to join an organisation with potential of expanding in the middle east region.

Michael Page