QC Chemical Analyst
Pubblicato il 21-08-2026 - Thermo Fisher Scientific in Milano
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
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Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting
Job Description
This role will:
Ensure continuity of GMP release testing activities supporting manufacturing and batch disposition (e.g: HPLC, UV, Karl Fisher).
Ensure timely execution of stability testing in accordance with regulatory commitments and approved stability programs.
Maintain laboratory capacity to support strategic customers, including MSD and Novo Nordisk, avoiding delays in product release and customer deliveries.
Support compliance with GMP requirements, internal procedures and data integrity expectations.
Mitigate the risk of increased workload on the existing analytical team, preventing delays, overtime, reduced flexibility and potential quality risks.
Main activities carried out by the QC Analyst:
Release Testing
Execution of routine GMP analytical testing for commercial batch release.
Documentation of analytical activities according to GMP requirements.
Review of analytical data and completion of laboratory documentation.
Investigation support for laboratory deviations and atypical results.
Stability Testing
Execution of stability analyses according to approved stability protocols.
Management of scheduled stability testing to ensure compliance with regulatory commitments.
Documentation and review of stability data
Other responsibilities
Support laboratory investigations (Deviations, OOS, OOT and LIRs).
Support equipment qualification, calibration and routine maintenance activities.
Execution of method verification activi