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QC CLEANING ANALYST

Descrizione dell'offerta di lavoro

Work Schedule Other 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 lifechanging 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 industryleading 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 with an increasing focus on biologics.
Joining more than colleagues on site the selected candidate will experience an excellent international and fastgrowing 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.
Joinin the QCCleaning team you will be part of a dynamic and resultdriven environment and you will gain and indepth experience of 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 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 team leader and supervisor SOPs and analytical procedures.
Perform other duties and support activities as assigned be compliant with all job related safety and other training requirements.
Provide testing support for production of sterile injectable.
Learn to perform analysis effectively and in GMP compliance mainly with Manage and dispose 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 English and italian languages (professional knowledge) Knowledge of the main chemical techniques (HPLC TOC UV...
Excellent knowledge of Office Suite Required Experience.
IC
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Dettagli dell'offerta

Azienda
  • Thermo Fisher Scientific
Località
  • Tutta l'Italia
Indirizzo
  • Imprecisato - Imprecisato
Tipo di Contratto
  • Imprecisato
Data di pubblicazione
  • 07/04/2025
Data di scadenza
  • 06/07/2025
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