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Review documentation related to microbiological tests, including bioburden and LAL tests, to verify compliance with required quality standards.
Evaluate and approve reports of sterility tests and endotoxin tests, ensuring accuracy, completeness, and adherence to procedures.
Critically analyze laboratory results provided by analysts and draft technical comments or requests for integration/correction.
Control and monitor microbiological quality control procedures, ensuring they are performed according to current regulations (GMP, ISO).
Interface with production and quality teams for technical clarifications and to ensure documentation accurately reflects compliance with sterility protocols.
Review and approve microbiological validation documentation related to instruments and processes.
Verify, update, and maintain technical documentation and standard operating procedures (SOP), ensuring consistency and compliance.
Work on a
continuous shift including nights .
Your Profile
Experience with microbiological tests: Bioburden , LAL test, endotoxin detection, sterility testing.
Knowledge of GMP and ISO regulations applicable to the pharmaceutical industry.
6 months/ 1 year of experience in similar roles in microbiological quality control.
Analytical and problem-solving skills in regulated environments.
Precision and attention to detail in laboratory activities and documentation.
Excellent teamwork and communication skills with various stakeholders.
Academic background: Degree in Biology or related disciplines (mandatory).
What We Offer
An international community bringing together 110+ different nationalities.
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibility.
A robust training system with our internal Academy and 250+ available modules.
A vibrant workplace that frequently gathers f
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