Work Schedule First Shift (Days)
Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards
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 100,000 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.
The 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.
Joining the Analytical Support and Validation team in the QC Lab, you will be part of a multifaceted environment and gain full experience in the introduction of new projects, technology transfer, and cleaning validation. Demonstrating your experience with chromatography and spectrophotometry, you will specifically focus on the following tasks:
Support in the implementation of protocols, reports, and documents, ensuring their management according to current GMP, SOPs, and guidelines.Perform analyses following specified instructions from team leader and supervisor, SOPs, and analytical procedures.Support activities as assigned, aligned with all job-related safety and training requirements.Provide testing support for the production of sterile injectable drugs.Learn and consolidate experience to work in GMP environments.Handle and dispose of samples.Prepare chemical solutions.How you will get there? Qualifications Previous experience in a GMP Laboratory.Ability to perform common chemical analysis; experience in HPLC, UV, and KF is strongly preferred.English and Italian languages (professional knowledge).Knowledge of the main chemical techniques (HPLC, GC, UV...).Excellent knowledge of Office Suite.
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