Work Schedule Every other weekend 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 RD in the industry, we give our people the resources and chances to create meaningful contributions to the world.
Joining the QC-Cleaning team, you will be part of a dynamic and result-driven environment and gain in-depth experience in a GMP Quality Control lab focused on cleaning analytical method development and validation, sampling, and analytical activities to guarantee the cleaning of manufacturing equipment to allow sterile processes on the production floor.
Leveraging your experience with chromatography, spectrophotometry, and TOC techniques, you will specifically focus on the following tasks: Support in the implementation of protocols, reports, and documents, and ensure their management according to current GMP, SOPs, and guidelines.
Perform analyses following specified instructions from the team leader and supervisor, SOPs, and analytical procedures.
Perform other duties and support activities as assigned, ensuring compliance with all job-related safety and other training requirements.
Provide testing support for the production of sterile injectable drugs.
Learn to perform analysis effectively and in GMP compliance.
Manage and dispose of samples preparing chemical solutions.
How you will get there?
Qualifications Previous experience in a GMP Quality Control lab.
Ability to perform common chemical analysis; experience in chromatography, TOC, and spectrophotometry is strongly preferred.
Experience in sampling of manufacturing equipment is preferred.
Professional knowledge of English and Italian languages.
Knowledge of the main chemical techniques (HPLC, TOC, UV...).
Excellent knowledge of Office Suite.
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