Aingeal L. Meagher, MsIT, MsITPM
Associate Quality Director
Over 15 years experience with Quality within Pharmaceutical and Biotechnology. Strengths include 21 CFR Part (Global Regulations around ERES). Extended expertise in Risk Management and Assessments, GAP Analysis, Validation (Iterative/Agile and V-Model Water-fall), Process Controls and Standard operation and processes/Procedures improvement. Extensive auditing experience: Internal, Vendor, Client and Global Agencies. Trained and provided training for GxP, ICH-GCP, EU, MDD and ISO, including other global standards.