Company:
A global biotechnology company dedicated to improving patients' lives through innovative medicines. The Breda manufacturing site is a highly automated, GMP-regulated facility responsible for the labeling, assembly, packaging, and global distribution of medicines to more than 75 countries worldwide. The company is committed to innovation, operational excellence, continuous improvement, and collaboration, while providing employees with excellent opportunities for professional growth and development.
Job Description:
We are seeking a Technical Operator (GMP) – Automated Manufacturing to join our advanced manufacturing team in Breda. In this role, you will play a key part in the day-to-day operation of automated production and packaging processes within a GMP-regulated environment, ensuring products are manufactured safely, efficiently, and to the highest quality standards.
Working closely with Production, Engineering, Maintenance, and Quality teams, you will operate advanced manufacturing equipment, troubleshoot technical issues, support continuous improvement initiatives, and help maintain reliable, compliant manufacturing operations. This position is ideal for someone who enjoys a hands-on technical role, solving problems, and contributing to a modern manufacturing environment where quality, safety, and operational excellence are central to everything we do.
Responsibilities:
• Ensure production activities are completed according to GMP, quality, and safety standards.
• Operate automated equipment used for manufacturing, assembly, labeling, and packaging activities.
• Prepare production lines for new batches, including equipment set-up, changeovers, cleaning, and line clearance activities.
• Review and record manufacturing data using digital systems such as SAP and Manufacturing Execution Systems (MES).
• Investigate process deviations and support Root Cause Analysis (RCA / 5 Why) to prevent recurring issues.
• Identify opportunities to improve workflows, equipment performance, and operational efficiency through Lean Manufacturing and Continuous Improvement initiatives.
• Work closely with Production, Engineering, Maintenance, and Quality teams to solve day-to-day operational challenges.
• Perform routine inspections, equipment adjustments, and basic first-line maintenance tasks.
• Monitor production performance and take appropriate action when abnormalities occur.
• Support a culture of teamwork, innovation, operational excellence, and continuous improvement.
Requirements:
• MBO-level technical qualification or equivalent experience.
• Experience working within manufacturing, production, processing, or other industrial operations.
• Experience operating or supporting automated machinery or technology-driven production environments.
• Strong problem-solving skills with a structured approach to troubleshooting.
• Previous experience within a GMP-regulated or other quality-controlled industry, such as pharmaceuticals, biotechnology, medical devices, food production, or chemicals.
• Knowledge of GMP requirements and quality-focused ways of working.
• Experience with production software or digital manufacturing systems such as SAP, MES, or similar platforms.
• A proactive attitude with a high level of ownership, accountability, and attention to detail.
• Good communication skills in English.
• Willingness to work a rotating 3-shift or 5-shift schedule.
Other Information:
This is an excellent opportunity to join a global biotechnology company and work in a highly automated, GMP-regulated manufacturing environment. You'll have the opportunity to contribute to the production and global supply of life-changing medicines while developing your technical expertise in a collaborative, innovative, and quality-driven workplace.
If you are interested in this opportunity and would like to apply, please submit your application via the apply button below or contact me for more information.
58501
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Manideep Rachakonda
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