Develop and maintain comprehensive production plans aligned with sales forecasts, inventory levels, and capacity constraints to ensure on-time delivery of medical devices (AEDs, monitors, etc.).
Conduct capacity planning and resource allocation, optimizing production schedules to maximize efficiency while adhering to quality and compliance standards (MDR, ISO 13485).
Lead material requirements planning (MRP), collaborate with procurement and warehouse teams to ensure timely availability of components, and minimize stock shortages or excess inventory.
Monitor production progress, identify bottlenecks, and implement corrective actions to address delays, quality issues, or supply chain disruptions.
Collaborate cross-functionally with R&D, quality assurance, sales, and manufacturing teams to align production plans with product launches, design changes, and regulatory updates.
Maintain production data and documentation (e.g., production schedules, capacity reports, material flow records) to support compliance audits and continuous improvement initiatives.
Support lean production initiatives, identify process optimization opportunities, and contribute to reducing lead times, waste, and production costs.
Ensure compliance with medical device regulations (MDR 2017/745) and internal quality management systems throughout the production planning process.

Bachelor’s degree or higher in Mechanical Engineering, Industrial Engineering, Supply Chain Management, or a related field.
Minimum 3 years of professional experience in production planning within the medical device industry (preferred) or high-tech manufacturing sector.
Proficiency in ERP systems (SAP HANA/R/3 is highly preferred) and production planning tools; strong data analysis and Excel skills.
Deep understanding of production planning principles, capacity management, MRP, and lean manufacturing methodologies (e.g., 5S, Kaizen).
Familiarity with medical device regulations (MDR, ISO 13485) and quality management systems in a manufacturing environment.
Excellent communication, coordination, and problem-solving skills, with the ability to collaborate effectively across cross-functional teams.
Detail-oriented, results-driven, and able to work under pressure to meet tight deadlines.
Fluent in Chinese, English and German (written and spoken) – mandatory for cross-border and internal collaboration.

Opportunity to work with a global leader in emergency medical technology, contributing to life-saving products.
Dynamic, collaborative, and compliant work environment with a focus on employee development and career growth.
Competitive salary package, including performance-based bonuses, health insurance, and retirement benefits.
Flexible working arrangements and professional training opportunities to enhance your skills in medical device production and compliance.
International exposure through collaboration with global teams across Europe, Asia, and the Americas.

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PRIMEDIC | Defibrillators made in Germany

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