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Laborant
Functieomschrijving
Role summary
In this role, you support GMP manufacturing activities in a controlled cleanroom environment in the Ghent region. You execute defined production process steps while strictly adhering to established procedures and documentation standards. Accuracy, discipline and compliance are key, as you ensure all activities are fully traceable and performed according to quality and safety requirements.
You work closely with colleagues from operations and support teams to deliver production according to a predefined shift schedule. In addition, you actively contribute to continuous improvement initiatives aimed at optimising processes and ways of working.
Key responsibilities
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Execute defined manufacturing process steps in a GMP-regulated cleanroom environment
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Apply strict aseptic and safety techniques during all operational activities
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Follow SOPs, batch records and work instructions accurately and consistently
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Complete GMP documentation to ensure full compliance and traceability
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Support the maintenance of production areas, including equipment cleanliness and environmental monitoring activities
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Collaborate with colleagues across teams to ensure smooth production flow according to the shift schedule
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Contribute to process improvements, efficiency initiatives and best practices
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Help maintain a safe, compliant and well-organised production environment
Practical information
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Location: Ghent region, Belgium
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Work pattern: Shift system (4 days on / 4 days off)
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Languages: Dutch or English
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Contract: Open-ended contract
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Compensation: Competitive salary package including fringe benefits (additional statutory vacation days, meal vouchers, group and hospitalisation insurance, double vacation pay, end-of-year bonus and performance-related incentives)
Profiel
Must-have requirements
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Bachelor’s or Master’s degree in sciences, bioengineering, biotechnology, pharmacy or a related field, or equivalent practical experience
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Ability to work precisely according to SOPs and detailed instructions in a regulated environment
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Fluency in Dutch or English, both written and spoken
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Willingness to work in a shift system
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Comfortable working in cleanroom conditions (gowning, disciplined and repetitive tasks)
Nice-to-have qualifications
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Experience in a GMP-regulated production or manufacturing environment
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Hands-on experience with aseptic techniques in cleanrooms
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Familiarity with GMP documentation practices such as batch records, logs and traceability systems
Soft skills & mindset
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Strong team player who can also work independently
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Clear and professional communicator
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Empathetic and respectful in daily collaboration
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Flexible and able to adapt to changing priorities
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Solution-oriented and proactive mindset
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Able to manage multiple tasks effectively
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Strong motivation to learn, grow and develop professionally
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