Automation Engineer

ARTO; Occitanie; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading automation company in France is seeking an experienced Automation Engineer to provide hands-on support across automation systems in a fast-paced GMP environment. Key responsibilities include leading FAT and SAT, supporting the validation life cycle, and collaborating with cross-functional teams. The ideal candidate has strong expertise with Siemens PLC7 systems and is fluent in French.

Qualifications

• Proven experience as an Automation Engineer within a GMP/CDMO or pharmaceutical environment.
• Strong technical expertise with Siemens PLC7 systems.
• Hands-on experience with FAT, SAT, commissioning, and validation life cycle activities.
• Ability to work independently and within cross-functional project teams under tight timelines.
• Fluency in French required; English proficiency is a strong plus.

Responsabilités

• Support automation activities related to facility and equipment within GMP manufacturing environments.
• Execute and troubleshoot Siemens PLC7-based systems.
• Lead and participate in FAT, SAT, and commissioning of automated equipment.
• Support the full validation life cycle, including protocol preparation, execution, and reporting.
• Collaborate with cross-functional engineering, validation, and operations teams to ensure project timelines and compliance are achieved.

Connaissances

Siemens PLC7 systems

Automation support

Validation life cycle

FAT and SAT

Independent work

Fluency in French

Description du poste

Overview

We are seeking experienced Automation Engineer who will provide hands-on support across automation systems, validation, and commissioning activities. This is a key contract position offering the opportunity to contribute to critical facility and equipment projects in a fast-paced GMP environment.

Responsibilities

• Support automation activities related to facility and equipment within GMP manufacturing environments.
• Execute and troubleshoot Siemens PLC7-based systems.
• Lead and participate in FAT (Factory Acceptance Testing), SAT (Site Acceptance Testing), and commissioning of automated equipment.
• Support the full validation life cycle, including protocol preparation, execution, and reporting.
• Collaborate with cross-functional engineering, validation, and operations teams to ensure project timelines and compliance are achieved.

Qualifications

• Proven experience as an Automation Engineer within a GMP/CDMO or pharmaceutical environment.
• Strong technical expertise with Siemens PLC7 systems.
• Hands-on experience with FAT, SAT, commissioning, and validation life cycle activities.
• Ability to work independently and within cross-functional project teams under tight timelines.
• Fluency in French required; English proficiency is a strong plus.