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