Automation Operator

SIRE LIFE SCIENCES; Breda; On-site; EUR 52,641 - 64,339; Full time

Job summary

SIRE LIFE SCIENCES is seeking an Automation Operator to operate, monitor, and optimize automated production lines in a GMP environment. You will troubleshoot, adjust parameters, and ensure accurate data recording in SAP and MES. The role supports continuous improvement and Lean initiatives while maintaining quality and safety.

The position requires experience with automated lines, SOPs/GMP, and strong English communication. Rotating shifts in a pharmaceutical manufacturing setting are expected.

Qualifications

• Minimum 3 years of experience in a similar manufacturing or production role.
• Experience working within automated production environments.
• Fluent English communication skills.
• Experience following SOPs and GMP procedures.
• Knowledge of assembly and packaging processes.
• Experience using SAP and MES systems.
• Strong troubleshooting and analytical skills.
• Experience with Lean Manufacturing and Six Sigma principles.

Responsibilities

• Operate and monitor automated production equipment according to SOPs and GMP standards.
• Perform troubleshooting and root cause analysis on automated systems.
• Adjust machine parameters and settings to improve operational performance.
• Record and verify production data within SAP and MES systems.
• Monitor process performance and report deviations when required.
• Complete batch records, production logs, and GMP documentation accurately.
• Participate in cross functional problem solving and triage meetings.
• Execute equipment startup and shutdown procedures.
• Perform routine cleaning activities according to production schedules.
• Identify and support continuous improvement opportunities.
• Contribute to Lean Manufacturing initiatives.
• Ensure smooth shift handovers and effective communication.
• Maintain a safe and compliant production environment.

Skills

Troubleshooting

Analytical thinking

Fluent English communication

Lean Manufacturing

Six Sigma

Mechatronics

Education

MBO/VAPRO B or equivalent

Tools

SAP

MES

Job description

The Company

A global pharmaceutical manufacturing organization focused on innovation, quality, and operational excellence. The company operates highly automated production facilities within a GMP regulated environment and invests heavily in advanced manufacturing technologies and continuous improvement initiatives.

Role Description

As an Automation Operator, you will be responsible for operating, monitoring, and optimizing automated production lines to ensure safe, efficient, and compliant manufacturing processes. This role combines technical troubleshooting, equipment operation, and GMP documentation while supporting process improvements and production performance.

Responsibilities

• Operate and monitor automated production equipment according to SOPs and GMP standards
• Perform troubleshooting and root cause analysis on automated systems
• Adjust machine parameters and settings to improve operational performance
• Record and verify production data within SAP and MES systems
• Monitor process performance and report deviations when required
• Complete batch records, production logs, and GMP documentation accurately
• Participate in cross functional problem solving and triage meetings
• Execute equipment startup and shutdown procedures
• Perform routine cleaning activities according to production schedules
• Identify and support continuous improvement opportunities
• Contribute to Lean Manufacturing initiatives
• Ensure smooth shift handovers and effective communication
• Maintain a safe and compliant production environment

Requirements

• Minimum 3 years of experience in a similar manufacturing or production role
• Experience working within automated production environments
• Fluent English communication skills
• Experience following SOPs and GMP procedures
• Knowledge of assembly and packaging processes
• Experience using SAP and MES systems
• Strong troubleshooting and analytical skills
• Experience with Lean Manufacturing and Six Sigma principles
• Technical understanding of mechatronics, pneumatics, and electronics
• Ability to understand and explain the function of sensors, valves, bearings, and automation components
• Willingness to work in rotating 3-shift or 5-shift schedules.
• Technical education such as MBO, VAPRO B, or equivalent

Other Information

• Shift based work environment
• Pharmaceutical manufacturing environment
• GMP regulated facility
• Strong focus on automation, quality, and continuous improvement

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