Microbiology Supervisor – Quality Control Department

A Pharmaceutical Company in Abu Dhabi, UAE (KEZAD) is looking for a Microbiology Supervisor – QC Department

Job Responsibilities

• Supervise and lead the QC Microbiology team, ensuring adherence to Good Manufacturing Practices (GMP) and company quality policies.
• Plan, assign, and monitor daily microbiological testing activities including sterility testing, bioburden analysis, endotoxin testing, microbial limits, and environmental monitoring.
• Oversee microbiological monitoring of controlled areas, cleanrooms, water systems (WFI, purified water), and compressed gases, ensuring compliance with regulatory standards.
• Review, analyze, and trend microbiological data, preparing timely reports for management and regulatory submission.
• Manage investigations related to Out of Specification (OOS), Out of Trend (OOT) results, deviations, and laboratory incidents, and ensure timely implementation of Corrective and Preventive Actions (CAPA).
• Ensure proper execution and documentation of method validation, method verification, and equipment qualification activities.
• Coordinate with cross-functional teams (Production, QA, Engineering) for contamination control and continuous process improvement.
• Prepare for and actively participate in internal, external, and regulatory audits (USFDA, EU, WHO, etc.), ensuring readiness of the microbiology lab.
• Maintain accurate documentation in compliance with GDP (Good Documentation Practices).
• Train, mentor, and develop team members to strengthen technical skills and regulatory knowledge.
• Ensure laboratory safety practices are strictly followed, with proper handling of biological materials and hazardous substances.

Job Qualifications

• Education:
  • Bachelor’s or Master’s degree in Microbiology.
  • Candidates with a degree in Pharmacy or Life Sciences with strong microbiology specialization may also apply.
• Experience:
  • 8–10 years of proven experience in pharmaceutical Quality Control microbiology.
  • Minimum 2–3 years in a supervisory or team lead role within QC microbiology.
• Technical Expertise:
  • Strong knowledge of microbiological testing methods, including sterility, endotoxin, microbial limits, and bioburden testing.
  • Expertise in environmental monitoring of classified areas, cleanroom management, and water system microbiology.
  • Hands-on experience with handling OOS/OOT investigations, deviations, CAPA, and change control processes.
  • Proficiency in method validation/verification, equipment qualification (LAFs, isolators, incubators, endotoxin systems), and laboratory management systems.
• Regulatory Knowledge:
  • In-depth understanding of international GMP regulations and guidelines (USFDA, EMA, WHO, MHRA).
  • Strong knowledge of documentation practices, regulatory compliance, and audit preparation.
• Skills:
  • Excellent communication and leadership skills to manage teams effectively.
  • Strong analytical and problem-solving abilities.
  • High attention to detail and ability to handle regulatory audits confidently.

Closing Date of Application : October 30 2025