Dave O'mara
About Dave O'mara
Dave O'Mara is an Associate QC Scientist at Bristol-Myers Squibb in Devens, Massachusetts, with experience in quality control and validation roles.
Current Roles at Bristol-Myers Squibb
Dave O'Mara holds multiple positions at Bristol-Myers Squibb in Devens, Massachusetts. He serves as an Associate QC Scientist, QCTS and also works as a Validation Consultant within the same department. Having started his tenure at Bristol-Myers Squibb in March 2019, Dave has been actively involved in quality control and validation roles. His responsibilities likely involve ensuring the integrity and compliance of pharmaceutical products and processes.
Current Role at Genzyme/Sanofi
Dave O’Mara is currently serving as the Principal Analyst in Quality Control at Genzyme, which operates under Sanofi. In this capacity, he is responsible for overseeing quality control procedures and ensuring that the products meet all the necessary standards and regulations.
Previous Roles at Genzyme/Sanofi
Before his current roles, Dave O'Mara worked at Genzyme, part of Sanofi, as the Principal Analyst in Quality Control. His experience in this position has provided him with extensive knowledge and expertise in quality control processes and methodologies within the pharmaceutical industry.
Experience in Quality Control and Validation
Dave O’Mara has significant experience in both Quality Control and Validation roles. This dual expertise enables him to ensure the quality and compliance of pharmaceutical products throughout various stages of the production process. His background includes roles that require keen attention to detail and thorough understanding of regulatory standards.