Microbiology QC Analyst (Sterile Environment)

About the role

El Kendi, part of MS Pharma, is looking for a Microbiology QC Analyst in a sterile environment in Algiers. The analyst performs microbiological analyses of raw materials, in-process products and finished products to ensure compliance with GMP requirements, product safety and the quality of biosimilar products. The role covers accurate testing, proper documentation, environmental monitoring and adherence to biosafety and data integrity standards.

Key responsibilities

• Perform microbiological control tests according to SOPs and validated methods
• Review and verify analytical results against established specifications
• Ensure strict application of GMP and biosafety requirements
• Document analyses, observations and test results in laboratory records and reports
• Maintain data integrity and traceability in line with ALCOA+ principles
• Clean, prepare and maintain microbiological equipment and instruments
• Carry out environmental monitoring (air, surfaces, purified water testing)
• Take part in instrument qualification and maintenance
• Identify and report OOS and OOT results
• Support investigations and CAPA implementation under the QC Supervisor
• Collaborate with QA and Production on non-conformities
• Take part in method transfer and validation, and support internal audits and regulatory inspections

Required profile

• Bachelor's to Master's degree (Bac +3 to Bac +5) in Microbiology, Biotechnology, Pharmaceutical Sciences or Laboratory Sciences
• 1 to 3 years of experience in pharmaceutical microbiology
• Knowledge of GMP / GxP environments; experience in biotechnology or biosimilar production is a plus
• Rigor, attention to detail, adherence to procedures, teamwork and strong sense of responsibility

Required skills

• Pharmaceutical microbiology techniques: culture, identification, sterility testing, endotoxin testing
• Good understanding of GLP and GMP requirements
• Handling of autoclaves, incubators, laminar flow hoods and microscopes
• Knowledge of laboratory documentation and data traceability