Quality Assurance Manager

General Information

Expertise Recruitment
Job Type:
Health Care/ Pharmaceutical
Date Posted:
Nov 05, 2023
Employee Type:
Full-Time Employee


• Bachelor's degree in life science (preferably in Pharmacy)
• 7+ years of proven experience as a Quality Assurance Manager in a cGMP and ISO-certified pharmaceutical manufacturing company.
• Fluent in Arabic and English.
• Extensive knowledge of cGMP, ISO standards, and regulatory compliance.
• Proficiency in policy development, audits, product quality management.
• Strong risk management and corrective action skills.
• Effective communication with regulatory bodies.
• Leadership, problem-solving, and team management abilities.
• Detail-oriented, analytical, and time-management skills.
• Commitment to ethical standards and continuous improvement.
• Optional certification in quality assurance.
• Adaptability and strong interpersonal skills for cross-functional collaboration.

• Oversee all activities related to quality assurance In the organization. This includes developing and implementing quality assurance policies, conducting audits, and ensuring that all procedures meet company and cGMP standards and ISO standards when applicable.
• Ensure compliance with cGMP regulations and other applicable quality standards. This includes staying updated with changes in regulatory legislation and guidelines.
• Responsible for ensuring the quality of the product through various stages of production, from raw materials to the finished product. This includes approving or rejecting drug batches based on quality control checks.
• Identify potential areas of compliance vulnerability and risk, develop and implement corrective action plans, and provide general guidance on how to avoid or deal with similar situations in the future. Oversee training and development programs to ensure that all employees are trained in cGMP and other relevant quality assurance procedures.
• Ensure that all necessary documents related to quality assurance are complete and up to date. This includes but is not limited to SOPs (Standard Operating Procedures), quality reports, validation reports, and regulatory submissions.
• Communicate with Regulatory Bodies.
• Drive continuous improvement initiatives across the organization and promote a culture of quality.

Company Profile