About Our Client
Our client is a leading global biopharmaceutical manufacturer, with a state-of-the-art production facility in Leiden. Known for producing high-quality biologics across a wide range of therapeutic areas, the organization operates within a highly regulated GMP environment.

Role Overview
You’ll support daily operations, solve problems on the production floor, and help improve quality, efficiency, and processes. Remote or hybrid work is not possible.

Responsibilities :

• Help fix daily issues in production
• Look into problems and find ways to reduce them
• Write and update procedures (SOPs)
• Support process and equipment improvements
• Work with teams to ensure safety, quality, and service
• Test new ideas, tools, and equipment
• Prepare documentation and training materials

Requirements:

• Vocational or technical education (preferred)
• 2â€"4 years in manufacturing or a similar environment
• Experience in a regulated industry is a plus
• Knowledge of GMP, ISO standards, and medical regulations
• Understanding of product and process validation
• LEAN Six Sigma Green Belt (preferred)

Other Information
Are you interested and do want to apply for this role, please fill out your application via the apply button below

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