Senior Process Engineer – Pharma Ops | Hybrid

Panda International; Breda; Hybrid; EUR 90,000 - 120,000; Full time

Job summary

Panda International in Breda seeks a Senior Process Engineer to drive optimization and operational performance within Warehouse and Logistics. You will implement data-driven solutions and coach colleagues to improve value streams.

You will independently manage multiple projects, collaborate with Quality Assurance, Engineering, Manufacturing and Logistics, and apply GMP/GDP knowledge in a highly regulated pharma environment.

Qualifications

• Bachelor's or Master's in Industrial Engineering or related field.
• Minimum 5 years in Industrial Engineering or process/performance improvement.
• At least 2 years in a highly regulated industry (Pharma, Chemistry or Food).
• Experience optimizing internal value streams.
• Good understanding of GMP and GDP.

Responsibilities

• Optimize internal value streams and warehouse/logistics processes.
• Analyze complex operational challenges using qualitative and quantitative data.
• Develop and implement new processes, methods and procedures to improve performance.
• Monitor, model and predict process performance using analytical tools.
• Anticipate potential problems and develop practical, sustainable solutions.
• Independently manage multiple projects and initiatives, aligned with business priorities.
• Collaborate with stakeholders across Quality Assurance, Engineering, Manufacturing and Logistics.
• Identify business needs and improvement opportunities through strong stakeholder relationships.
• Provide coaching, training and guidance to colleagues.

Skills

Analytical thinking

Problem solving

Stakeholder management

Cross-functional collaboration

Coaching

Education

Industrial Engineering degree

Tools

Analytical tools

Job description

Panda International in Breda seeks a Senior Process Engineer to drive optimization and operational performance within Warehouse and Logistics. You will implement data-driven solutions and coach colleagues to improve value streams.

You will independently manage multiple projects, collaborate with Quality Assurance, Engineering, Manufacturing and Logistics, and apply GMP/GDP knowledge in a highly regulated pharma environment.