GMP Automation Engineer - Pharma & Biotech

agap2 Switzerland; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Training with accredited centers

Local management support

Zusammenfassung

agap2 Switzerland is seeking an Automation Engineer to design, implement and qualify automation solutions in GMP environments on-site with leading pharmaceutical and biotech clients. You will collaborate with engineering, production, quality and validation teams on complex projects.

Minimum 2 years in GMP-regulated pharma/life sciences and hands-on experience with PLC/SCADA/HMI/DCS/MES or OT networks is required. Proficiency in English is essential; German is a strong advantage.

Qualifikationen

• Degree in Automation, Electrical Engineering or a related field.
• Minimum 2 years of GMP-regulated pharma/biotech life science experience.
• Experience with PLC/SCADA/HMI/DCS/MES or OT networks.
• Knowledge of GMP, GAMP 5, data integrity and qualification/validation principles.

Aufgaben

• Design, develop and implement automation solutions in GMP environments.
• Contribute to the configuration and programming of PLC, HMI, SCADA, DCS or MES systems.
• Support FAT, SAT, commissioning, qualification and validation activities.
• Troubleshoot automation, control and communication issues.
• Develop and improve automation standards, procedures and technical documentation.
• Support batch control, recipe management, data integrity and process monitoring activities.
• Coordinate with multidisciplinary teams, suppliers and client stakeholders.
• Contribute to the delivery of strategic pharmaceutical and biotech projects.

Kenntnisse

PLC

SCADA

HMI

DCS

MES

Industrial OT networks

Troubleshooting

Analytical skills

Independent work

English communication

Ausbildung

Degree in Automation

Electrical Engineering degree

Tools

Siemens

Rockwell Automation

Emerson DeltaV

Syncade

Jobbeschreibung

agap2 Switzerland is seeking an Automation Engineer to design, implement and qualify automation solutions in GMP environments on-site with leading pharmaceutical and biotech clients. You will collaborate with engineering, production, quality and validation teams on complex projects.

Minimum 2 years in GMP-regulated pharma/life sciences and hands-on experience with PLC/SCADA/HMI/DCS/MES or OT networks is required. Proficiency in English is essential; German is a strong advantage.