Interpret and implement quality assurance standards.
Evaluate the adequacy of quality assurance standards.
Document internal audits and other quality assurance activities.
Investigate customer complaints and non-conformance issues.
Develop, recommend, and monitor corrective and preventive actions.
Identify training needs and organize training interventions to meet quality standards.
Coordinate and support on-site audits conducted by external providers.
Evaluate audit findings (internal or external audits) and implement appropriate corrective actions.
Assure ongoing compliance with quality and industry regulatory requirements.
Analyze records of product returns to identify specific problems or trends over time.
Prepare documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, and corrective actions.
Prepare all quality department SOPs.
Ensure that manufacturing processes comply with GMP standards at both national and international levels.
Requirements:
Familiar with the laws and requirements of pharmacovigilance in pharmaceutical companies.
Proficient in the regulatory affairs of the Food and Drug Organization, preparing documents and files to send/register to the Ministry of Health.
Mastery of the Chargoon and TTAC systems for registering pharmaceutical products, supplements, and raw materials.
Proficiency in English
Doctor of Pharmacy.
At least 4 years of experience as a quality assurance manager in a pharmaceutical manufacturing company.
Leadership skills.
Problem-solving skills.
Communications and interpersonal skills.
Attention to detail.
Analytical thinking.
Maturity.
Result oriented.
Excellent documentation skills.
Fluent in English.
Excellent MS Office knowledge (Excel, Word, PowerPoint).
Good numerical skills and an understanding of statistics.
Familiar with local regulatory affairs and EU GMP standards.