Divide the work between the people under supervision and monitor how they work.
Develop executive plans in line with the company's goals and strategies.
Establish a quality assurance committee in accordance with the relevant instructions and existing conditions.
Supervise the proper implementation of quality assurance of equipment and systems according to the latest available and valid guidelines.
Supervise matters assigned to the documentation center, including requests to create, modify, delete, review, and distribute copies of the entire organization.
Monitor the proper implementation of Product Quality Review (PQR) and Quality Risk Management (QRM).
Carry out the necessary studies and reviews regarding the implementation of GXP improvement programs and provide solutions.
Coordinate with supervised staff to conduct periodic GXP inspections and internal audits.
Monitor the handling of deviations, controlling changes, and corrective actions issued to determine the task of the mentioned cases.
Requirements
At least 5 years of managerial experience in pharmaceutical companies.