Ross Glidden
About Ross Glidden
Ross Glidden is a Downstream Manufacturing Lead at Bristol-Myers Squibb and a Validation Specialist at PharmEng Technology, with over a decade of experience in the pharmaceutical and biotechnology industries.
Downstream Manufacturing Lead at Bristol-Myers Squibb
Ross Glidden currently serves as a Downstream Manufacturing Lead at Bristol-Myers Squibb. In this role, he is responsible for overseeing downstream processes in the manufacturing of biopharmaceutical products. His duties likely include ensuring the quality and efficiency of the production process, managing resources, and maintaining compliance with industry standards. Glidden brings extensive experience to this position, having worked in the pharmaceutical and biotechnology industries for over a decade.
Validation Specialist at PharmEng Technology
Since September 2019, Ross Glidden has been working as a Validation Specialist at PharmEng Technology. His responsibilities in this role involve ensuring that all systems and processes comply with regulatory standards and operate efficiently. This includes validating equipment, processes, and software systems crucial for pharmaceutical production. His expertise in validation supports the ongoing quality and compliance in the manufacturing operations he oversees.
Senior Manufacturing Associate at Sanofi Genzyme
Ross Glidden worked at Sanofi Genzyme as a Senior Manufacturing Associate from 2010 to 2016. Located in Allston, Massachusetts, his role involved advanced manufacturing duties in the biotechnology sector. For six years, he contributed to the production processes and likely took part in improving manufacturing protocols and maintaining high standards of product quality and safety.
Education: Associates from Great Bay Community College
Ross Glidden holds dual associate degrees from Great Bay Community College, completed during two distinct periods (2001-2003 and 2008-2010). These academic credentials provided him with foundational knowledge and technical skills essential for his roles in the pharmaceutical and biotechnology industries. The specialized education from Great Bay Community College has been instrumental in shaping his career and professional development.
Professional Background in Pharmaceutical and Biotechnology Industries
Ross Glidden has accumulated over a decade of experience in the pharmaceutical and biotechnology sectors. His career includes significant roles in manufacturing and validation, contributing to companies such as Sanofi Genzyme, PharmEng Technology, and Bristol-Myers Squibb. His roles have ranged from Senior Manufacturing Associate to Downstream Manufacturing Lead and Validation Specialist, showcasing his versatility and depth of expertise in the field.