Coordinator, NPI Micro Lab

Overview Work Schedule: Standard (Mon-Fri). Environmental Conditions: Laboratory Setting. Job Description Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier cleaner and safer. Whether our customers are accelerating life sciences research solving sophisticated analytical challenges growing efficiency in their laboratories improving patient health through diagnostics or the development and manufacture of life-changing therapies we are here to support them. Our global organization of more than 100000 colleagues delivers an outstanding combination of innovative technologies purchasing convenience and pharmaceutical services through our industry-leading brands including Thermo Scientific Applied Biosystems Invitrogen Fisher Scientific Unity Lab Services Patheon and PPD. Monza site is an outstanding pharmaceutical contract manufacturing and development facility specialized in aseptic injectable drugs with a growing focus on biologics. Joining more than 1800 colleagues on site the selected candidate will experience an excellent international and fast-growing environment. With revenues exceeding $24 billion and the largest investment in R&D in the industry we give our people the resources and chances to create meaningful contributions to the world. How will you make an impact As QC Micro NPI Coordinator you will join the QC Microbiological Lab reporting to the laboratory team leader. Using your technical and analytical skills you will support Grade-A sterile production operations by ensuring the quality control microbiology testing. You will thrive in a fast-paced team of professionals passionate about sterile drugs production and for delivering life-saving drug products to patients across the world! Responsibilities support the team leader to coordinate the NPI Micro team support for the scheduling of testing support the team for microbiological method validation (bioburden endotoxin sterility) for in process samples incoming materials finished product samples in accordance with the cGMP and presenting in a timely manner to the team leader any anomalies execute validation for microbiological methods perform microbiological laboratory activities issue laboratory documentation (validation protocol and report OOS / deviation record laboratory investigation SOP) work in support of sterile production departments Qualifications Preferable MSc in biology or biotechnology Good Italian and English Level (written and spoken) Attention to details strong organizational skills, the ability to multi-task and effective interpersonal and communication skills are important. Key Skills Catering Apache Commons Architectural Design Human Resources Administration Accident Investigation Employment Type Full-Time Experience years Vacancy 1 J-18808-Ljbffr

Location: Monza, Lombardia, IT

Posted Date: 9/16/2025