Ophthalmic Packaging Equipment Technician

Novartis Farmacéutica

Conza della Campania

In loco

EUR 28.000 - 36.000

Tempo pieno

5 giorni fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

Novartis is seeking an Equipment Operator to ensure secondary packaging of ophthalmic products in a GMP environment. You will operate automated lines, perform set-up and changeover, and monitor materials and equipment to maintain quality and efficiency.

Responsibilities include line clearance and in-process controls, data verification for serialisation, and supporting investigations and audits. You will work with QA, MS&T, engineering and maintenance to sustain operations and drive improvement.

Competenze

  • Technical diploma or equivalent; experience in pharma packaging is a plus.
  • Strong focus on GMP compliance and quality documentation.
  • Willingness to work in shifts and participate in training.

Mansioni

  • Operate automated secondary packaging lines for ophthalmic products, including set-up and start-up.
  • Manage feeding of packaging materials and monitor equipment performance.
  • Perform Line Clearance, Line Checks, and in-process controls for quality.
  • Verify coding, serialization, aggregation and readability of data; handle non-conforming products.
  • Comply with GMP, Data Integrity and HSE; ensure traceability and proper production docs.
  • Support investigations and participate in audits and inspections.
  • Collaborate with QA, MS&T, Engineering and Maintenance on line cleaning and continuity.
  • Contribute to continuous improvement, operational excellence, and waste/deviation reduction.

Conoscenze

Attention to detail
Teamwork
Problem solving
Compliance awareness

Formazione

Technical high school diploma or equivalent (Mechanical/Electrical/Electronic/Chemical)

Strumenti

MES
SAP

Descrizione del lavoro

Novartis is seeking an Equipment Operator to ensure secondary packaging of ophthalmic products in a GMP environment. You will operate automated lines, perform set-up and changeover, and monitor materials and equipment to maintain quality and efficiency.

Responsibilities include line clearance and in-process controls, data verification for serialisation, and supporting investigations and audits. You will work with QA, MS&T, engineering and maintenance to sustain operations and drive improvement.

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