| Location | Breda, Netherlands |
|---|---|
| Business Sector | Biotechnology |
| Contact name | Daria Finikova |
| Contact email | |
| Job ref | 25208 |
| Published | about 12 hours ago |
Overview:
We are looking for a results-driven and knowledgeable Process Operator to join our high-performance production team. You will be responsible for operating advanced equipment in a GMP-controlled and regulated environment, ensuring the production of high-quality medicines for our patients. You bring a strong technical and analytical skillset, a continuous improvement mindset, and a mature, proactive attitude. You take pride in your work, thrive in dynamic settings, and are energized by working with high-tech systems and contributing to a meaningful mission.
You will operate within the ABR production hall, which houses nine (semi-)automated production lines. Each line is managed by a team of 3–9 skilled operators. Together, your team ensures the safe, accurate, and efficient execution of production processes in compliance with GMP regulations and quality standards.
Key responsibilities include change-over procedures, monitoring process parameters, troubleshooting, reporting deviations, data analysis, and maintaining consistent performance. You will work closely with production supervisors, line leads, and key stakeholders to ensure process excellence and continuous improvement.
Operate production equipment in line with SOPs and GMP standards
Document and analyze process data in SAP/MES systems
Ensure timely, high-quality product output and smooth line performance
Monitor, anticipate, and respond to process deviations or atypical events
Communicate clearly with teammates and line leads to meet shared goals
Take ownership of shift handovers and ensure seamless information transfer
Participate in continuous improvement initiatives (LEAN, Six Sigma)
Support related logistics processes and compliance tasks
Stay current with all mandatory training and certifications
Work Experience:
10+ years in a manufacturing environment as a process/technical operator (GMP, GDP, or ISO-certified environment preferred)
5+ years working with LEAN, Six Sigma, and continuous improvement methodologies
Hands-on experience with 5WHY, RCA, Kaizen, Poka Yoke, TPM, ATS, SMED, Fishbone
Certified in Lean Six Sigma (Yellow or Green Belt)
Experience working with SAP, MES, and ERP systems
Familiarity with Standard Operating Procedures and quality systems
Education:
MBO in a technical or process discipline
AND/OR
VAPRO A and B certification
Advanced LEAN or Six Sigma training/certification
Proficiency in Microsoft Office (Word, Excel, PowerPoint)
Fluent in Dutch and English, both verbal and written
Team-oriented and collaborative
Structured and detail-oriented
Accountable and results-driven
Strong analytical thinking and problem-solving skills
Clear and effective communication
Demonstrates ownership and follow-through
Adaptable to shifts, overtime, and weekend schedules
Respectful, trustworthy, and committed to quality
Eager to learn and continuously improve
Self-reflective with a growth mindset
Comfortable working in diverse teams and multicultural environments
Proactive and open to change
Able to work independently on improvement projects
This role offers an opportunity to contribute meaningfully to a mission-driven organization focused on delivering high-quality medicines to patients worldwide. If you’re ready to take ownership of your work, thrive in a team setting, and grow within a LEAN-driven environment, we’d love to hear from you.