COORDINATOR, NPI MICRO LAB

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 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 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! What will you do 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 insupport of sterile production departments; Skills Preferable MSc in biology or biotechnology Good Italian andEnglish Level (written and spoken) Attention to details strong organizational skills the ability to multi-task and effective interpersonal and communication skills are important.
Thermo Fisher Scientific is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race creed religion color national or ethnic origin citizenship sex sexual orientation gender identity and expression genetic information veteran status age or disability status.
Required Experience.
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