Niamh has over 20 years’ experience in international medical device and pharmaceutical manufacturing in particular Quality Management Systems. Niamh started her career as a Pharmaceutical Analyst in R&D before taking up a position as a QC Chemist with an international bulk pharmaceutical manufacturer. Niamh then moved to the medical device sector working for a leading medical device company where she held the position of QC Manager for 12 years gaining extensive experience in all aspects of Quality Management including auditing and regulatory affairs compliance. While undertaking a BA in Pharmaceutical Business Operations, Niamh was particularly interested in regulatory affairs and clinical trials and decided to move into this area. Niamh is now working as a Regulatory Affairs consultant with Real Regulatory having joined the company in 2016.
Niamh holds a B.Sc. in Analytical Science from DCU and a BA in Pharmaceutical Business Operations from Griffith College & Innopharma Labs.
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