Quality Associate at CLS MedPharma
As the Quality Associate in CLS Medical Device & Pharma Testing, Miriam supports and advises in the development and implementation and management of the quality system within the company, which includes all quality control, quality assurance and quality improvement activities. She is the individual responsible for regulatory inspection preparation activities and was the host of the successful HPRA audit in June 2012 for GMP compliance and the FDA inspection in March 2014.
With her many years’ experience, Miriam has developed a wide variety of skills and knowledge which she utilises in establishing strategic plans, systems, policies and procedures at all levels for maintaining high standards of quality performance, reliability and safety within CLS Medical Device & Pharma Testing.
Miriam is a BSc graduate from NUIG with over 20 years experience in the pharmaceutical and medical device industries.