• University Degree in Business, Sciences, or Engineering with previous experience overseeing site operational readiness activities, ideally in CDMO for Viral Vector, Cell Therapy, Antibody, or Vaccine production; 
• 10+ years of experience in the biopharmaceutical industry with 5+ years managing cell and gene therapy production entities; 
• Technical proficiency in scaling up manufacturing processes (10 L to 200 L batches); 
• Aseptic handling and cleanroom operations experience; 
• Demonstrated leadership with direct team supervision; 
• Exceptional organisational skills in fast-paced environments; 
• Strong attention to detail and adaptability to changing priorities. 

This is an opportunity to join an exciting CDMO with a mission to translate research and early-stage clinical programs into actionable health solutions for patients. You can expect the following from the organisation:

• You will have the opportunity to lead a cutting-edge, state-of-the-art facility and be a crucial part of the organisation’s growth; 
• Competitive renumeration package with good secondary benefits.