I’m partnering with a leading global biopharma to find an Analytical Subject Matter Expert for a career-defining role in the EU/UK. 
Key highlights include:
Driving regulatory submissions (including BLAs)
Leading analytical method development, tech transfer, and validation
Spearheading CMC and Quality Management initiatives
Collaborating cross-functionally on cutting-edge biologics projects
Shape the future of biologics with a global biopharma leader! Let’s connect this week to discuss how this aligns with your ambitions. My schedule is open, and interviews are set to begin early next week after an initial screening with me.
Please reach out to me at to explore this incredible opportunity!