Manufacturing Process Technician, Breda, Noord-Brabant

Location: Breda, Noord-Brabant  |  Sector: Biotechnology  |  Start Date: 7/28/2026  |  Job ref: 58327

The Company
A leading pharmaceutical manufacturing organization specializing in high quality medical products within a highly regulated GMP environment. The company operates advanced automated production lines and focuses on continuous improvement, operational excellence, and delivering safe and effective medicines to patients.

Role Description
The Manufacturing Process Technician is responsible for operating and optimizing production lines in a controlled and regulated environment. The role focuses on maintaining high quality standards while ensuring process efficiency and continuous improvement. You will work closely with operators, line leads, and supervisors to ensure smooth operations and consistent output

Responsibilities
- Run and oversee automated manufacturing equipment while ensuring compliance with GMP guidelines and standard operating procedures (SOPs)
- Diagnose equipment issues and support root cause investigations to minimize production downtime
- Optimize machine settings and process parameters to improve efficiency and product quality
- Enter, maintain, and verify production information in SAP and MES systems
- Track production performance and escalate process deviations when necessary
- Complete production records, batch documentation, and GMP-related paperwork with accuracy
- Collaborate with production, engineering, and quality teams to resolve operational challenges
- Carry out equipment start-up, changeover, and shutdown activities following established procedures
- Perform routine cleaning and basic maintenance tasks in line with production schedules
- Identify process improvement opportunities and contribute to operational excellence initiatives
- Support Lean Manufacturing and continuous improvement projects
- Ensure effective communication during shift transitions to maintain production continuity
- Follow all health, safety, and compliance requirements to maintain a safe working environment


Requirements
- At least 3 years of experience in a manufacturing, production, or process operations role
- Hands-on experience working with automated production equipment
- Strong command of the English language, both written and spoken
- Familiarity with GMP regulations and adherence to SOP-driven environments
- Experience in assembly, packaging, or high-volume manufacturing processes
- Practical knowledge of SAP, MES, or similar production management systems
- Strong analytical mindset with proven troubleshooting and problem-solving abilities
- Understanding of Lean Manufacturing, Six Sigma, or continuous improvement methodologies
- Technical knowledge of automation systems, including mechatronics, pneumatics, and electrical components
- Ability to interpret the operation of sensors, actuators, valves, bearings, and other automation equipment
- Flexible to work rotating 3-shift or 5-shift schedules
- Technical qualification such as MBO, VAPRO B, or an equivalent vocational education


Other Information
- Shift-based position within a pharmaceutical production facility
- Work in a GMP-regulated manufacturing environment
- Exposure to highly automated production systems
- Strong emphasis on quality, safety, compliance, and continuous improvement initiatives

58327

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Mohammed Sarfaraz

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