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Manufacturing Process Technician (GMP) | 3 shifts | Breda

LocationBreda, - None Specified -
Business SectorBiotechnology
Contact nameDaria Finikova
Contact email
Job ref26556
Publishedabout 4 hours ago

Description

The Manufacturing Process Technician is responsible for operating and optimizing high-tech, semi-automated pharmaceutical production lines in a GMP-regulated environment. The role focuses on safe and compliant line operation, data-driven process control, and continuous improvement to ensure timely delivery of high-quality medicines to patients.


Sectors

Pharmaceutical Manufacturing / Life Sciences


Company Size & Type

Large, highly regulated pharmaceutical manufacturing site with multiple semi-automated production lines.


Must Have Requirements

  • ?10 years experience as a process or technical operator in a manufacturing environment
  • Experience in GMP, GDP, or ISO-certified environments

  • ?5 years hands-on experience with LEAN / Continuous Improvement methodologies

  • Lean or Six Sigma Yellow or Green Belt certification

  • Experience with ERP/MES systems (SAP and/or MES)

  • Experience working with SOPs and regulated procedures

  • MBO education in technical or process field and/or VAPRO A/B

  • Fluent Dutch and English (verbal and written)

  • Availability for 3-shift work, including weekends and overtime


Desirable Requirements

  • Advanced LEAN or Six Sigma training

  • Experience with tools such as: 5WHY, RCA, Kaizen, Poka Yoke, TPM, SMED, Fishbone

  • Experience in pharmaceutical or high-end medical manufacturing

  • Strong data analysis skills at operator level

  • Experience working in multicultural production teams


Responsibilities

  • Operate semi-automated production lines according to GMP and SOPs

  • Monitor, adjust, and fine-tune process parameters to ensure product quality

  • Perform changeovers and support equipment troubleshooting

  • Record, analyze, and document process data in SAP/MES

  • Identify and implement process improvements using LEAN principles

  • Escalate deviations and atypical events according to procedures

  • Ensure accurate shift handovers and documentation

  • Collaborate closely with operators, line leads, and production supervisors

  • Support logistics-related production activities

  • Ensure all required training is completed within deadlines

  • Actively participate in continuous improvement and root cause analysis activities

    Interested? Send your CV to Daria at d.finikova@panda-int.com or call +31202044502 for more info.