Production Technician

Location: Saluggia

Work in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation.

About

The Role

Key responsibilities include:

Control of Raw Materials (MP) for the manufacturing of the sterile batch (e.g. labels, shelf‑life, compliance with  ).

Prepare in the Sterile Area product bulk solutions and set up the machine for filling, stoppering and crimping vials, execute production activities in Sterile Area, according to the Batch Record instructions, aseptic behavior instructions and SOPs, label and package the products.

Participate in the Media Fill execution.

Observe behavioral standards and flow of materials in the areas with controlled contamination (and with regard to the sterile room) in compliance with the internal procedures.

Sterilize in an autoclave and dry caps and capsules in the oven according to the internal procedures; de‑aerate flasks and glassware in the oven to be used in the subsequent processing phases.

Perform cleaning and washing of the glassware and bottles to be used in the subsequent processing steps in accordance with the procedures laid down by the specific procedures.

Perform visual inspection, manually and using the semi‑automatic screamer machine.

Keep track in a timely manner of all the activities performed during the manufacturing process, as per Data Integrity, SOPs instruction and GMP requirements.

Essential Requirements

Scientific/technical background.

Experience in production or quality department in a manufacturing environment within the pharmaceutical industry.

Fluent in Italian. Good knowledge of English.

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