Production Supervisor - Homeopathic Products & Process Engineer

GREEK NATURAL BEAUTY, POWERED BY SCIENCE KORRES is a Greek skincare brand, born out of Athens’ oldest homeopathic pharmacy in 1996. Founded by Greek Pharmacist George Korres who believes in the innate potency of natural ingredients and chemical engineer Lena Philippou who believes that nature is the inspiration for scientific discovery. Inspired by the most powerful natural ingredients and local traditions, KORRES delivers effective natural products; discovered in nature and nurtured by science. KORRES collaborates with over 15 different European academic universities to do ground-breaking research into the power of plants. Our research shapes and nurtures nature’s inherent powers. Today KORRES takes Greek herbs around the world through more than 400 natural products, with brand presence in 30 markets. It is all about clean, effective plant-powered formulas that capture the beauty of Greece in harmony with nature. KORRES is looking for a dynamic and self-motivated Production Supervisor – Homeopathic Products & Process Engineer to join the Homeopathic Department . Key Responsibilities Production planning, inventory monitoring, and coordination of manufacturing activities to ensure operational efficiency and product availability. Management of production orders, raw material consumption, labor hours, and production documentation. Supply and stock monitoring of raw materials and production consumables, including supplier evaluation and qualification. Ensuring compliance with GMP/GDP requirements, ISO standards, internal audits, and regulatory inspections. Oversight of production and warehousing operations in accordance with approved procedures, quality standards, and regulatory requirements. Approval and implementation of SOPs and review of production documentation prior to batch release. Coordination of equipment maintenance, qualification, validation, and operational readiness of new machinery. Monitoring production KPIs, manufacturing data analysis, and operational reporting. Implementation of process optimization and digital transformation initiatives to improve productivity and operational performance. Ensuring compliance with environmental policies, ISO 14001 standards, and environmental management procedures. Coordination and continuous training of production personnel to support compliance and operational excellence. Driving continuous improvement initiatives across production, quality, compliance, and operational processes.

Bachelor’s degree in Pharmacy, Medicine, Chemistry, Pharmaceutical Chemistry & Technology, or Biology. Minimum 2 years of relevant experience in pharmaceutical manufacturing, quality assurance, or quality control environment. Experience in GMP/GDP regulated production environments. Proficient user of Microsoft Office and SAP systems. Fluent in English, both written and spoken. Knowledge of TPM, 5S, and EH&S principles. Strong analytical, reporting, organizational, and problem-solving skills. Team-oriented mindset with effective communication and people management skills. Continuous improvement and process optimization orientation.