Manufacturing Process Technician
SIRE® Life Sciences
Manufacturing Process Technician
Samenvatting
Wat krijg je?
Wat ga je doen?
- Operate automated equipment following SOPs
- Perform troubleshooting and root cause analysis
- Adjust machine parameters to optimize performance
- Record production data in SAP systems
- Complete GMP documentation and batch records
Wat verwachten wij?
- Technical education such as MBO or VAPRO B
- Three years experience in a manufacturing environment
- Experience with automated production systems
- Experience in pharmaceutical or food manufacturing
Volledige vacaturetekst
At this global leader in biopharmaceutical manufacturing, you will operate and optimize highly automated production lines where high-quality medicines are crafted. You play a key role in technical troubleshooting and process optimization within a sophisticated GMP environment. Join a team that invests heavily in operational excellence and advanced technology to improve patient lives. Dive into the world of high-tech pharma and contribute to life-changing production.
The Company
A global leader in biopharmaceutical manufacturing focused on producing high quality medicines that improve patient lives. The organization operates within a highly regulated environment and invests heavily in automation, operational excellence, and continuous improvement to ensure compliance and efficiency.
About the Role
As a Technical Operator, you will be responsible for operating, monitoring, and optimizing highly automated production lines within a GMP regulated manufacturing environment. You will play a key role in ensuring production targets, product quality, equipment reliability, and regulatory compliance are consistently achieved.
This position combines technical troubleshooting, process optimization, documentation, and cross functional collaboration with Quality Assurance, Maintenance and Engineering, and Production teams.
Responsibilities
• Operate and monitor automated production equipment following SOPs and GMP requirements
• Perform advanced troubleshooting and root cause analysis on equipment and processes
• Adjust machine parameters and mechanical settings to optimize performance
• Record and verify production data within SAP and MES systems
• Analyze process performance and escalate deviations when necessary
• Complete GMP documentation including batch records and production logs
• Participate in triage meetings with QA, Maintenance and Engineering, and Production teams
• Carry out equipment setup and shutdown activities
• Execute daily, weekly, and monthly cleaning procedures
• Monitor equipment performance and identify improvement opportunities
• Support Lean and continuous improvement initiatives
• Ensure effective shift handovers and team communication
• Maintain a safe, compliant, and organized working environment
Requirements
• Minimum 3 years of experience in a production or manufacturing environment
• Experience working with automated production systems
• Experience within assembly, packaging, pharmaceutical, food, or similar manufacturing environments
• Technical education such as MBO, VAPRO B, or equivalent
• Knowledge of GMP standards and SOP driven environments
• Experience with SAP and MES systems
• Strong troubleshooting and root cause analysis skills
• Familiarity with Lean Manufacturing, Six Sigma, and continuous improvement methodologies
• Knowledge of mechatronics, pneumatics, and electronics
• Ability to work effectively in structured and regulated environments
• Strong communication and teamwork skills
• Fluent English language skills
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