The QC Technician performs analysis on batches and incoming materials according to cGMP rules and SOPs.
Job Description
Major accountabilities :
* Perform analysis of batches following specific training.
* Promptly report to the Quality Control Supervisor and the Qualified Person any deviations or out-of-specification results detected during analysis.
* Collaborate with the Quality Control Head/Supervisor for CAPA implementation in the department.
* Control processes, equipment, and area.
* Perform routine maintenance, cleaning, and microbiological verification of pharmaceutical QC equipment; support external specialists in maintenance/qualification activities.
* Verify incoming and outgoing materials.
Collaborate with the Quality Control Head on material stock and waste management, as well as training new personnel.
* Execute calibration, verification, qualification, and validation activities for QC processes and equipment.
Essential requirements :
* Scientific Degree (preferably in Pharmacy, Chemistry, or related fields).
* Experience in a similar role within the pharmaceutical or chemical industry.
* Availability to work shifts, including nights and weekends.
* Fluent in Italian with good knowledge of English.
We offer a temporary contract as a starting point.
Additional information :
Novartis is committed to diversity and inclusion, fostering an inclusive work environment. We offer benefits and opportunities for professional growth.
Skills include: Continued learning, decision-making, industry standards, laboratory techniques, Qc testing, TQM, and more.
Required Experience :
Key Skills : Laboratory experience, aseptic technique, ELISA, FDA regulations, PCR, HPLC, microbiology, GLP, cGMP, LIMS, QA/QC.
Employment Type : Full-Time
Experience : [Specify years]
Vacancy : 1
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