Panda International
jobid=A.0.0407
As a Specialist Production Operator, you will be responsible for executing production activities in the manufacturing process of EllanséTM 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.
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.
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.
Role Competencies:
- Strong attention to detail and accuracy
- Organized and methodical approach to work
- Quality-driven mindset
- Critical thinker
General Competencies:
- Team-oriented and supportive
- Patient and adaptable
- Calm and effective under changing conditions
- Empathetic and respectful in team communication
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
