Quality Assurance Manager

We are hiring a Quality assurance manager!

We are seeking an experienced Quality Assurance Manager to oversee all aspects of our QA operations, including GLP compliance, SOP management, and external site supervision.

Key Responsibilities

• Manage and maintain GLP compliance for in vivo studies
• Oversee non-GLP studies to ensure adherence to GLP principles where applicable
• Develop, implement, and maintain company-wide SOPs
• Supervise QA activities for external collaborating sites
• Lead and coordinate QA audits for internal and external operations
• Guide preclinical studies towards successful IND submissions (both in-vivo and in-vitro)
• Ensure compliance with OECD guidelines and GLP standards
• Train staff on GLP requirements and quality assurance practices
• Liaise with regulatory bodies and clients on quality-related matters

Qualifications

• Master's degree in Biology or related life science field (required)
• Minimum 2 years of experience in the preclinical industry
• Demonstrated experience leading GLP preclinical studies 
• In-depth knowledge of GLP regulations, OECD/ICH guidelines
• Strong understanding of in vitro and in vivo preclinical study designs
• Excellent project management and communication skills
• Ability to work effectively with internal teams and external partners

Preferred Skills

• Familiarity with international regulatory requirements (FDA, EMA, etc.)
• Knowledge of quality management systems and risk assessment methodologies
• Good communication skills, multitasking and leadership

Location: Ness Ziona

Candidates are welcome to send their CV to: [email protected]

Please indicate "QA" in the mail's title