The Opportunity

What You’ll Do 

• Maintaining an electronic system for conducting training

• Managing quality complaints, conducting investigations, CAPA (corrective and preventive actions and providing personal feedback)

• Assessment (auditing or surveying) and monitoring of supplier KPIs that may affect quality

• Supporting Quality Management System documents (SOPs, training)

• Participating in internal and supplier audits

• Responding to requests from regulatory authorities regarding certification

Requirements:

• Higher education (pharmaceutical, technical (engineer, biotechnologist), standardization and certification)

• 1–1.5 years of experience in pharmaceutical manufacturing, warehousing, quality assurance, registration, pharmacovigilance

• English – Intermediate

• Good MS Office skills (MS Word, MS Excel, PowerPoint)

• Attention to detail, open to new knowledge, compliant.