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Quality Assurance Manager

1.00 to 10.00 Years   Amman, Jordan   03 Apr, 2022
Job LocationAmman, Jordan
EducationNot Mentioned
SalaryNot Mentioned
IndustryOther Business Support Services
Functional AreaNot Mentioned

Job Description

- Quality Assurance Manager Company: Industry: Pharmaceuticals Job Location: Amman, Jordan Career Level: Upper Management (Manager, Director, Head) Date Posted: 29-03-2022 Ref. Number: 150560 Citizenships Jordan Residence Country Jordan Years of Experience 10 - 16Quality Assurance Manager and Requirements Participating in the development of strategies and objectives of the department. Developing and managing the execution of short term plans for implementing the approved objectives. Flourishing suggestions and recommendations that would enable a more effective and efficient work flow. Flourishing suggestions and recommendations that would enable a more effective and efficient work flow. Participating in developing the departments budgets and managing the activities within towards achieving the set budget. Developing managerial and technical circulars within the department towards the achievement of the set plans and objectives. Conducting periodic meetings with subordinates regarding work priorities and ensuring work is flowing smoothly. Assessing and approving all changes in materials; equipment, facilities or processes based on proper assessment and ensure that all change requirements are addressed to demonstrate that the quality of the products is not adversely affected by these changes. Reviewing and approval of all documentations of all batches to ensure that they have been manufactured and tested in compliance with CGMP, marketing Authorization and regulatory affairs changes prior to release for sale. Approving product annual review for all products Following up of the clients complaints/ recalls system, and ensure that complaints are handled properly and corrective/ preventative actions are taken as deemed necessary. Ensuring that the products are stored, distributed and handled so that quality is maintained throughout their shelf life. Establishing a system of self inspection and external auditing to verify that CGMP and other regulations are applied throughout the plant and to follow up on corrective actions. Responsible for all in process control procedures and activities. Responsible for safety and health occupational procedures and activities. Assuring the management that the companys operations especially the core operations (manufacturing, supplies ,controls, etc.) are being conducted in accordance with plans, processes and standards (e.g. CGMP System requirements), and the relevant authorities regulations (e.g. government regulations for pharmaceutical manufacturing are met. Monitoring and auditing work practices to ensure processes are being followed and products are reviewed/tested/inspected to ensure that high-quality product is being produced. Reducing risk levels in operations by defining processes and ensuring that they are complied. Monitoring adherence with GMP requirements Monitoring adherence with safety rules within the facility. Implementing of documented quality systems at all levels. Ensuring total compliance in quality front with respect to customer/ regulatory agencies

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