Quality Documentation Coordinator | Pharmaceutical Industry | Jerusalem
Strong English writing skills and an eye for detail? Join the Quality Department of a leading pharmaceutical company and help maintain the documentation that supports manufacturing quality and regulatory compliance.
📍 Jerusalem | Full-time
What you’ll do:
- Manage the site’s document control system, including creating, updating, reviewing and distributing controlled documents.
- File and archive quality records, batch documentation and production logbooks, and maintain retained-sample inventory records.
- Track employee training and qualifications through the electronic Quality Management System (eQMS).
- Coordinate and support internal audits, supplier audits and regulatory inspections.
- Write, edit and translate quality documents, including Product Quality Reviews (PQRs).
- Support process improvements and compliance with GMP and ISO requirements.
What you’ll bring:
- Native-level English, with excellent writing skills, and full proficiency in Hebrew.
- Excellent command of Microsoft Word and Excel.
- Strong organizational skills, accuracy and accountability.
- The ability to work independently, prioritize tasks and collaborate across departments.
- Availability for a full-time position in Jerusalem.
An advantage:
- A degree in life sciences, biology, chemistry, biotechnology, pharmaceutical sciences or quality-related studies.
- Previous experience in quality assurance, quality documentation or a GMP, biotech or medtech environment.
- Familiarity with eQMS.
What’s on offer:
A stable workplace in the pharmaceutical industry, meals, a Ten Bis meal benefit and employee benefits.
