Quality Manager

We're looking for a Quality Manager to lead our QMS and regulatory processes as we scale innovation in cell therapy manufacturing — the ideal candidate is a hands-on leader with deep experience in ISO 13485, FDA compliance, and a passion for operational excellence in biotech.

Key Responsibilities:

• Oversee QMS processes, including ISO 13485, CE, and FDA compliance.
• Manage audits, document control, CAPA, customer complaints, and supplier evaluations.
• Collaborate with cross-functional teams to drive quality improvements and process excellence.

Qualifications:

• 5+ years in QMS and regulatory affairs, with 3+ years in a leadership role.
• Experience with cell therapy, pharma, and single-use components.
• Strong communication skills in English and Hebrew.
• Join us to shape quality and innovation in the medical device industry!