Ireland
Quality Operations Manager External Manufacturing
Pharmaceuticals
Experience
Bristol-Myers Squibb January 2013 - Present
Skills
Regulatory Requirements, Laboratory, 21 CFR Part 11, Biopharmaceuticals, Drug Development, GAMP, Pharmaceutical Industry, Regulatory Submissions, Cleaning Validation, Aseptic Processing, Biotechnology, Sterilization, LIMS, Computer System..., SOP, Clinical Trials, Quality Auditing, Software Documentation, Quality System, Vaccines, Technology Transfer, Aseptic Technique, Analytical Chemistry, Quality Assurance, V&V, Manufacturing, FDA, Trackwise, Deviations, Quality Management, GMP, Quality Control, Validation, Pharmaceutics, Regulatory Affairs, Lifesciences, Change Control, Cell Culture, GLP, Sop, GxP, Chromatography, CAPA