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