Product specialist (operator)

Job Overview:

As a Specialist Production Operator, you will be responsible for executing production activities in the manufacturing process of Ellansé™ dermal filler, specifically within Microspheres, Aseptic Processing, Visual Inspection, or Final Packaging. You will act as a subject matter expert, ensuring the highest standards of GMP compliance, product quality, and process reliability, while also supporting and training team members.

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Key Responsibilities:

Production Execution

• Ensure proper execution of all assigned production processes.

• Take ownership of production steps and guarantee consistent output quality.

• Report on production progress, status, and issues.

Training & Coaching

• Train and coach coworkers in various process steps and GMP best practices.

• Support colleagues in case of improper behavior or incorrect process execution.

Quality & Compliance

• Ensure strict adherence to GMP, ISO, and internal quality standards.

• Immediately report any deviations or non-conformities to the Supervisor or Production Manager.

• Demonstrate excellent GMP documentation skills and help foster GMP awareness within the team.

Documentation & Authorization

• Sign as second operator after completion of primary training (e.g., batch record verification).

• Accurately complete all production and quality-related documentation.

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Main Tasks:

• Perform key tasks typically handled by the Supervisor when delegated.

• Take control of production processes and ensure they run according to standards.

• Maintain performance standards and actively contribute to a culture of excellence.

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Role Competencies:

• Strong attention to detail and accuracy

• Organized and methodical approach to work

• Quality-driven mindset

• Critical thinker

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General Competencies:

• Team-oriented and supportive

• Patient and adaptable

• Calm and effective under changing conditions

• Empathetic and respectful in team communication

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Required Skills & Qualifications:

Essential:

• Proven experience in a production environment (preferably life sciences or pharmaceuticals)

• Ability to speak, read, and write in English

Desirable:

• Prior experience working in GMP, ISO, or similarly regulated environments

• Experience with training or mentoring junior operators

• Proficiency in Dutch (spoken and written) is an advantage