Niamh Flynn

Pharmaceutical Professional with 5+ years’ experience in GMP-regulated environments spanning Manufacturing, Quality Control, and Stability. Skilled in compliance, sample management, aseptic techniques, and process support, with a proven track record of establishing a new stability programme at a start up site. Recognised for adaptability, problem-solving, and cross-functional collaboration in both biologics and sterile manufacturing settings.

I have 5 years of experience in GMP regulated environments, mostly in the pharmaceutical industry. I have experience in both manufacturing and quality in industry leading companies such as Pfizer, MSD and CSL Seqirus. 

I have a BSc. In Biomedical Science from Maynooth University and then completed a certification in Industrial Microbiology and Pharmaceuticals while working full time.