QC Analyst

4 settimane fa

Monza, Lombardia, Italia Thermo Fisher Scientific Inc. A tempo pieno

Work Environment

At Thermo Fisher Scientific Inc., we are 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.

Joining Monza site, an outstanding pharmaceutical contract manufacturing and development facility, specialized in aseptic injectable drugs, with an increasing focus on biologics, 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.

Job Responsibilities

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 team leader and supervisor, SOPs and analytical procedures.
  • Provide testing support for production of sterile injectable drugs.
  • Learn to perform analysis effectively and in GMP compliance, mainly with chromatography, spectrophotometry and TOC techniques.
  • Manage and dispose samples preparing chemical solutions.

Requirements

  • 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.
  • English and Italian languages (professional knowledge).
  • Knowledge of the main chemical techniques (HPLC, TOC, UV...).
  • Excellent knowledge of Office Suite.

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