Lead the setup, implementation, and day-to-day operation of a GMP-compliant microbiology laboratory
Oversee microbiological testing activities, including bioburden, sterility, endotoxin testing, microbial identification, environmental monitoring, and water testing
Define and maintain microbiology standards to ensure compliance with EU GMP, FDA.
Develop, implement, and maintain the laboratory Quality Management System (QMS), including SOPs, test methods and policies.
Design, implement, and maintain environmental monitoring programmes, including sampling plans
Environmental Monitoring Data Management include charting, analyzing data, interpreting the overall monitoring process behavior, detecting a trend or shift in contamination levels, monitoring excursion rates.
Participate in the development of the Contamination Control Strategies
training staff in aseptic manufacturing process to address regulations to prevent microbiological contamination of the pharmaceutical product.
Collaborate with cross-functional teams to ensure an effective cleaning validation program and participate in disinfection programs development.
Ensure laboratory audit readiness and support internal, client, and regulatory inspections.
Lead and support deviations, investigations, and non-conformances
Qualifications
Bachelor’s degree in Microbiology, Biology, or related field. Master's degree is a plus.
Proven experience in a laboratory leadership or management role
Strong knowledge of GMP standards and expertise in microbial identification, testing techniques, and laboratory instrumentation.
Strong knowledge of Risk-based approaches through the subsequent ICHQ9 guideline on risk management for the manufacture of sterile pharmaceutical products.
Excellent problem-solving skills with strong attention to detail
Strong communication skills, both written and verbal, in Greek and English