Pharma Automation Engineer – GMP Systems & IT

Bracco Suisse S.A.; Plan-les-Ouates; Presencial; CHF 90 000 - 120 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive remuneration

First-class benefits

Resumo da oferta

Bracco Suisse S.A. is seeking an Automation Specialist for our Geneva site in Plan-les-Ouates.

You will ensure availability and reliability of computerized production systems, support operations, and drive digitalization projects within a highly regulated pharmaceutical manufacturing environment. You will manage GMP-compliant automation, administer industrial IT networks, and lead lifecycle management of production equipment systems.

Qualificações

• Degree in Automation Engineering or Electrical/Electronics field.
• Experience in pharmaceutical or regulated environments preferred.
• Strong knowledge of Siemens S7 PLCs, TIA Portal and SCADA (iFIX/FIX32).
• Familiarity with industrial IT: networks, Windows domains, servers, VMware.
• Rigorous, quality-driven and compliant mindset; proactive and collaborative.

Responsabilidades

• Manage and maintain computerized systems in GMP-compliant way.
• Administer industrial IT and production networks on site.
• Lifecycle management of production equipment computerized systems.
• Review audit trails and support compliance activities.
• Lead IT, automation and digitalization projects.
• Maintain technical docs and quality procedures for systems and networks.
• Interface with corporate IT, telecom and automation stakeholders.
• Provide expertise on PLCs, servers, vision, printing systems and industrial software.
• Manage maintenance contracts for computerized systems.

Conhecimentos

Siemens S7 PLCs

TIA Portal

SCADA (iFIX/FIX32)

Industrial IT infrastructure

GMP awareness

French/English

Teamwork

Formação académica

Degree in Automation Engineering

Electrical/Electronics Engineering

Ferramentas

VMware

Windows Server

iFIX/FIX32 SCADA

Descrição da oferta de emprego

Bracco Suisse S.A. is seeking an Automation Specialist for our Geneva site in Plan-les-Ouates.

You will ensure availability and reliability of computerized production systems, support operations, and drive digitalization projects within a highly regulated pharmaceutical manufacturing environment. You will manage GMP-compliant automation, administer industrial IT networks, and lead lifecycle management of production equipment systems.