QA Auditor

IMP Clinical Supply Services Ltd. is a prominent company in the field of clinical trial supply management that specializes in providing comprehensive, tailor-made clinical supply chain management services that address all study phases and regulatory requirements.
We are currently seeking a QA Auditor to join our QA team.
Responsibilities:
· Oversee secondary packaging, distribution and clinical supply activities.
· Verify, investigate, and support processes and conformance to QA standards including: Good Manufacturing Practice (cGMP), Good Distribution Practice (GDP), as well as customer requirements.
· Review, prepare, and update Standard Operating Procedures (SOPs), Master Packaging Instructions, forms, and other controlled documents.
· Review and approve Packaging/Labeling batch records.
· Handle deviations, investigations, complaints, internal and external audits, and CAPA performance.
· Support daily Clinical Supply activities.
· Support the update and customization of the ERP system for end-users.
· This is a full-time, on-site position. The Company's office is located in Modi'in Region Industrial Park, near Shoham.
Qualifications:
· Working Proficiency in Hebrew and English – a must.
· Strong written and communicative skills in Hebrew and English – a must.
· Attention to detail, thorough, and customer-service oriented disposition – a must.
· BSc in Life Sciences or related field – a must.
· Previous QA experience in GMP/GDP environment – an advantage.
· Knowledge of the clinical trials field and Good Clinical Practice – an advantage.
· Familiarity with ERP systems and database environments – an advantage.
· Experience working directly with customers and independently, meeting deadlines, and multitasking – an advantage.