مدیر کنترل کیفیت

Job Description

Key Responsibilities:

• Plan, organize, and supervise all activities within the QC laboratories
• Review and approve analytical test results for raw materials, in-process, and finished products
• Ensure calibration, maintenance, and performance qualification of laboratory equipment
• Review and approve QC documentation including SOPs, analytical methods, and test reports
• Collaborate with Quality Assurance (QA) for deviation investigations, CAPA processes, and audits
• Act as the primary liaison with the Food and Drug Organization (FDO) and other regulatory bodies for inspections and documentation
• Train, coach, and evaluate QC personnel to ensure technical and regulatory compliance
• Ensure strict adherence to GMP, GLP, and other applicable global quality standards

Job Requirements:

• Education: MSc or Pharm.D. or PhD in Pharmacy, Chemistry, Pharmaceutical Chemistry, Microbiology, Biology, or related fields
• Work Experience: Minimum 8 years of relevant experience in QC laboratories within the pharmaceutical industry, including at least 3 years in a managerial or supervisory role
• Certifications: Completion of GMP, GLP, Quality Management, Risk Management, and Advanced HPLC training courses (certified is a plus)
• Language Proficiency: Strong command of technical English (reading, writing, and communication)
• IT Skills: Familiarity with lab software systems (e.g., Empower, LIMS) and Microsoft Office tools