GMP Automation Engineer – Pharma IT & PLC Expert

Bracco Medical Technologies; Plan-les-Ouates; On-site; CHF 90,000 - 130,000; Full time

Benefits offered by this job

Bright prospects

First-class benefits

Job summary

Bracco Medical Technologies in Geneva area seeks an Automation Specialist to ensure availability, reliability and compliance of computerized production systems. You will support operations, lead improvement projects and drive digitalization in a pharmaceutical manufacturing environment.

Reporting to the Maintenance & Engineering Manager, you will manage automation projects, maintain GMP-compliant systems, and coordinate with IT and automation stakeholders across the site.

Qualifications

• Degree in automation or related engineering field.
• Experience in regulated pharma or similar industries.
• Strong knowledge of industrial automation systems.
• Familiar with IT infrastructure, networks, Windows domains and VMware.

Responsibilities

• Manage and maintain computerized systems in GMP environment.
• Administer site industrial IT and production networks.
• Oversee lifecycle of production equipment computerized systems.
• Review audit trails and support compliance activities.
• Lead IT, automation and digitalization projects.
• Maintain documentation and quality procedures for systems and networks.
• Interface with corporate IT, telecom and automation stakeholders.
• Provide expertise on PLCs, servers, vision systems and industrial software.
• Manage maintenance contracts for computerized systems.

Skills

Siemens S7 PLCs

TIA Portal

SCADA iFIX/FIX32

Industrial IT infrastructure

Windows domains

Servers

VMware environments

Networking

French & English

Education

Automation/Electrical Engineering degree

Tools

TIA Portal

iFIX/FIX32

Job description

Bracco Medical Technologies in Geneva area seeks an Automation Specialist to ensure availability, reliability and compliance of computerized production systems. You will support operations, lead improvement projects and drive digitalization in a pharmaceutical manufacturing environment.

Reporting to the Maintenance & Engineering Manager, you will manage automation projects, maintain GMP-compliant systems, and coordinate with IT and automation stakeholders across the site.