First seen by Alion on Sep 25, 2026. SIRE Life Sciences scores B on the Alion truth index.
The company
Our client is a leading international organisation involved in the manufacturing, packaging, storage, and distribution of medicines worldwide. The organisation operates in a highly regulated environment, with a strong focus on safety, quality, compliance, operational excellence, and continuous improvement.
Role Description
As a Technical Production Operator - Automated Manufacturing, you will be responsible for operating, monitoring, and optimising automated production systems in a GMP-regulated environment. You will combine technical expertise with operational discipline to maintain equipment performance, ensure product quality, and support continuous improvement initiatives.
Responsibilities
- Operate and monitor automated production equipment and manufacturing lines.
- Perform equipment set-ups, changeovers, line cleaning, and line clearances in accordance with established procedures.
- Troubleshoot process disturbances and take appropriate action to restore production performance.
- Maintain production equipment and perform minor mechanical adjustments where required.
- Document and verify production data accurately using SAP and/or MES systems.
- Support deviation management and participate in production and quality triage activities.
- Contribute to continuous improvement initiatives using Lean and structured problem-solving methodologies.
- Ensure production processes are performed safely, efficiently, and in compliance with GMP and quality requirements.
- Adjust mechanical and process parameters to optimise equipment and production performance.
- Perform root cause analysis using methodologies such as RCA and 5WHY.
Requirement
- MBO or equivalent technical education.
- Proven experience in an automated production environment, preferably within assembly, labelling, packaging, or similar manufacturing operations.
- Strong technical, mechanical, and analytical skills.
- Experience with structured troubleshooting and root cause analysis methodologies, such as RCA and 5WHY.
- Experience working in a highly regulated manufacturing environment; GMP experience is preferred.
- Familiarity with SAP and/or MES systems.
- Strong sense of ownership with a structured and quality-driven approach to work.
- Fluent in English, both written and spoken.
- Willingness and flexibility to work in 3-shift and 5-shift operations.
Other information
Looking for a new opportunity in automated manufacturing? Well, it's right here! If you're interested, please click the below button to apply for the job.
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