The Company
A global leader in pharmaceutical manufacturing with a strong focus on innovation, quality, and patient safety. The organization operates highly automated production facilities and is committed to maintaining the highest standards of compliance, operational excellence, and continuous improvement.
Role description
As an Automated Line Operator, you will be responsible for operating, monitoring, and optimizing advanced automated production lines within a GMP regulated environment. This role combines technical knowledge, troubleshooting expertise, and process improvement skills to ensure safe, efficient, and high quality manufacturing operations. You will work closely with Production, Quality, and Engineering teams to support operational performance and compliance.
Responsibilities
- Operate and monitor automated production equipment according to SOPs and GMP standards
- Perform troubleshooting and root cause analysis to resolve equipment and process issues
- Adjust machine settings and operating parameters to optimize performance
- Record, verify, and maintain production data in SAP and MES systems
- Review process performance and escalate deviations when required
- Complete GMP documentation including batch records and operational logs
- Participate in problem solving and triage meetings with Quality, Maintenance, and Production teams
- Perform equipment setup, line changeovers, and shutdown activities
- Execute daily, weekly, and monthly cleaning activities
- Monitor equipment efficiency and identify improvement opportunities
- Support Lean Manufacturing and continuous improvement initiatives
- Ensure effective shift handovers and communication between teams
- Maintain a safe, compliant, and organized working environment
Requirements
- Minimum 3 years of experience in a manufacturing or production environment
- Experience operating automated production equipment
- Experience within assembly, packaging, pharmaceutical, food, or similar industries
- Fluent English communication skills
- Comfortable working within a structured environment governed by strict procedures
- Willingness to work in a shift based schedule
- Experience working with GMP documentation and compliance requirements
- Strong troubleshooting and analytical skills
- Experience with SAP and MES systems
- Knowledge of Lean Manufacturing and continuous improvement practices
- Experience with root cause analysis tools such as 5 Why, Fishbone, Kaizen, TPM, SMED, and Poka Yoke
- Understanding of mechatronics, pneumatics, electronics, sensors, valves, -bearings, and automated systems
- Technical education such as MBO, VAPRO B, or equivalent
Other Information
If you are interested and want to apply, please submit your application via the apply button below and contact me.
59004
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Mohammed Sarfaraz
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