Are you eager to contribute to the manufacturing? of innovative treatments? Join a cutting-edge biotechnology company specializing in cell therapies. In a highly regulated GMP environment, you will supervise the production of advanced therapies. This role places you at the heart of manufacturing life-changing solutions for patients.

Mission

You will be directly responsible for supervising production operations. You ensure quality, regulatory compliance, and the efficiency of manufacturing processes within a GMP framework.

Responsibilities

• Lead production teams and support their development
• Ensure compliance with cGMP standards and participate in quality inspections
• Manage and review critical documentation (SOPs, work instructions, batch records)
• Oversee batch release and associated quality controls
• Collaborate with cross-functional departments to resolve production issues
• Initiate continuous improvement projects (efficiency, cost, quality)

Profile

• Degree in science, bio-engineering, pharmacy or equivalent
• Minimum 3 years of experience in a GMP or ATMP environment
• Knowledge of aseptic operations and MES/EBR tools
• Fluent in English (spoken and written)
• Strong leadership, attention to detail, and ability to manage priorities

What We Offer

• A role with direct impact on patient health
• An innovative and international work environment
• A competitive salary package with numerous fringe benefits
• Pay attention that it’s a SHIFT system