Akim Yildiz

-Product implementation -Optimization Projects

Disciplinary responsibility for personnel Subject matter responsibility: - Responsibility acc. to §14 AMWHV - Implementation raw material analytics - Cleaning validation - Planning of special analytics - Qualification of analytical equipment - Material management system for Quality Control - GMP- und Food Compliance QC

Point of contact for customer, working with national and international customers, Coordination of analytics, process validation and commercialization, Project cost tracking

Qualification as Expert Pharmacist for Pharmaceutical Analytics

Supplier Qualification, Specification incoming goods, Risk assessment of raw materials and finished products, PQR, Compliance of pharmaceutical and food products

Information coordination between involved parties, Project planning, Representative of the Quality Department towards customers (national and international), Performance reporting to the General Management, Process Validation

Development, optimization and validation of routine analysis in a GMP environment - with a focus on HPLC analysis. Qualification of analytical equipment, storage and production facilities and manufacturing equipment. Revision and further development of the quality management system.

Department of Pharmaceutical Development Identification, implementation and validation of state-of-the-art container closure testing method