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Microbiological quality control analyst

Siena
Experteer Italy
Pubblicato il Pubblicato 8h fa
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PpOpen positions /p pJob Title: MICROBIOLOGICAL QUALITY CONTROL ANALYST /p pLocation: Siena - Italy /p pDepartment: Quality Control Analytical /p h3Position Overview /h3 pPhilogen S.p.A. is a biotechnology company dedicated to developing targeted products for the imaging and treatment of life‑threatening diseases with a strategic focus on oncology. Our mission is to translate cutting‑edge scientific innovation into effective therapies that improve patients' lives. Philogen S.p.A. is seeking a Microbiological Quality Control Analyst to join the Quality Control Department. The successful candidate will perform microbiological testing and environmental monitoring activities in compliance with Good Manufacturing Practice (GMP) standards, supporting the quality and safety of our biopharmaceutical products. /p h3Key Responsibilities /h3 ul liPerform microbiological analytical methods, including bioburden testing, Growth Promotion Test (GPT), Mycoplasma detection, biological indicator testing, and sterility testing. /li liConduct environmental monitoring activities in classified manufacturing areas, including sampling, incubation, and testing. /li liPerform sampling and microbiological testing of water systems (Water for Injection, Clean Steam, Purified Water, Softened Water, and Drinking Water). /li liExecute microbiological quality control of finished products and in‑process samples. /li liPrepare, review, and maintain protocols, reports, and Standard Operating Procedures (SOPs). /li liCompile and manage data forms, registers, and certificates in accordance with internal procedures. /li liEnsure proper management, calibration, and maintenance of laboratory instruments. /li /ul h3Requirements /h3 ul liDegree in Biology, Biotechnology, Pharmacy, or a related scientific discipline. /li liSolid scientific background and technical competence in microbiological analyses. /li liProven experience in a similar role within a GMP‑regulated pharmaceutical or biotechnology environment. /li liStrong knowledge of GMP principles and quality system requirements. /li liExcellent attention to detail, with the ability to prioritize tasks and manage workload efficiently. /li liCapability to work independently and to coordinate team members when required. /li liStrong interpersonal and communication skills, with a collaborative and proactive attitude. /li /ul h3What We Offer /h3 ul liA professional and supportive work environment focused on scientific excellence and teamwork. /li liA contract and salary commensurate with the candidate's experience and seniority. /li liOpportunities for professional development within an innovative and growing biotechnology company. /li /ul h3Job Location /h3 pSiena - Italy /p pWe invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief. /p /p #J-18808-Ljbffr

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