Alexandra Aviles Sirett
About Alexandra Aviles Sirett
Alexandra Aviles Sirett is a Manager and Quality Assurance Scientist at Bristol Myers Squibb in Manati, Puerto Rico, with extensive experience in the pharmaceutical industry.
Current Role at Bristol Myers Squibb
Alexandra Aviles Sirett is currently positioned as the Manager, Quality Assurance Scientist (QA Support) Eng, Whse & Supply Chain at Bristol Myers Squibb. She took on this role in December 2021 and is based in Manati, Puerto Rico. Her current responsibilities involve overseeing quality assurance processes within the engineering, warehousing, and supply chain departments to ensure compliance with industry standards and regulatory requirements.
Experience with Amgen
Alexandra Aviles Sirett has an extensive history with Amgen, where she served in various quality assurance roles. From 2019 to 2021, she worked as a QA Specialist with RCM Technologies in Juncos, PR. Earlier in 2019, she briefly held the position of Quality Specialist Complaints at Amgen (Consultant RCM TECH) in Juncos, PR for two months. Additionally, she was a QA Specialist from 2013 to 2014 at Amgen's Juncos, PR site.
Tenure at Teva Pharmaceuticals
Alexandra Aviles Sirett worked at Teva Pharmaceuticals in Florida for several years. She served as a Quality Assurance Engineer II from 2016 to 2018 in Davie, Florida, focusing on improving QA processes and ensuring compliance with regulatory standards. Prior to that, she worked as a Quality Assurance Engineer I from 2014 to 2015, where she was responsible for various quality assurance tasks aimed at maintaining product integrity.
Long-Standing Role at Pfizer
Alexandra Aviles Sirett spent 12 years at Pfizer as a QA Specialist / QC Scientist. This role, which she held from 2000 to 2012 in Carolina, PR, involved handling quality control and assurance tasks. She played a key role in ensuring that products met rigorous quality standards and adhered to U.S. FDA regulations.
Educational Background
Alexandra Aviles Sirett acquired her Bachelor's degree in Biology and Microbiology from the University of Puerto Rico. She pursued her studies from 1994 to 1999, equipping herself with the foundational knowledge required for her accomplished career in quality assurance within the pharmaceutical industry.
Quality Assurance Expertise
Alexandra Aviles Sirett possesses extensive experience in Quality Assurance, particularly in Good Laboratory Practice (GLP) and Good Distribution Practices (GDP). She has strong skills in Change Control, U.S. FDA regulations, Corrective and Preventive Action (CAPA), and Quality Auditing, making her a valuable asset in ensuring product quality and regulatory compliance.