Minőségbiztosítás állások Külföldön középiskolai végzettséggel

• Execute test protocols in laboratory environment. 
• Report test results and nonconformities in a timely manner. Stock management and delivery. 
• Support the follow-up and documentation of stock moves (e.g., inventory check).
• Support the preparation of delivery orders. Laboratory equipment management.

• Kennenlernen des vollumfänglichen Herstellungsprozesses eines Medikaments – von der Rohstoffverarbeitung bis zur Verpackung
• Arbeiten in einer der modernsten Produktionsanlagen Europas für Arzneimittel
• Begleitung durch erfahrene Teams, die ihr Know-how in der Herstellung fester Arzneiformen weitergeben

• Preparation of production facility for underwater equipment.
• Manufacturing and finishing of parts to be used in products.
• Development of manufacturing aids based on OEM descriptions.
• Incoming goods inspection and quality control of internally manufactured goods.

• Perform daily business in technical and administrative aspects
• Support Production (Shift) Team Leaders to ensure appropriate skill level of production and SCM teams in all quality-related process aspects

Following up on production-related nonconformities, supporting root cause analyses, defining and monitoring corrective actions, and preparing evaluations and statistics of nonconformities...

• Rationalization and improvement of production technology as well as warehousing and distribution processes
• Continuous improvement of existing products in cooperation with the technology department and production units

• Provides direct supervision, resolves personnel issues, conducts performance evaluations, and performs managerial discipline, as necessary.
• Directly reports to include quality control supervisors.

• Serve as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Complaint Management and Recall within the EUCAN region.
• Lead the regional standardization and harmonization of Complaint Management and Recall processes, ensuring alignment with GMP and GDP requirements.

• Serve as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Deviation, CAPA, and OOx within the EUCAN region.
• Drive the standardization and harmonization of these processes at a regional level, ensuring alignment with both GMP and GDP requirements.