Mejias Jose
About Mejias Jose
Mejias Jose is the Parenteral Inspection and Packaging Senior Supervisor at Bristol-Myers Squibb, with over 20 years of experience in the chemical, pharmaceutical, and bio-pharmaceutical industries.
Current Title and Role
Mejias Jose currently holds the position of Parenteral Inspection and Packaging Senior Supervisor at Bristol-Myers Squibb, located in New Jersey, United States. In this role, he oversees the inspection and packaging processes for parenteral products, ensuring compliance with Good Manufacturing Practices (GMP's) and FDA regulations.
Previous Experience at Pfizer
Mejias Jose worked at Pfizer as a Manufacturing Supervisor from 2008 to 2010 in New York, New York, United States. During his time at Pfizer, he was responsible for overseeing the manufacturing processes, ensuring high standards of safety, and regulatory compliance within the production environment.
Previous Experience at Amgen
From 2004 to 2008, Mejias Jose served as a Front Line Manager in the Packaging Department at Amgen in Thousand Oaks, California, United States. He was tasked with managing the packaging operations ensuring efficiency and compliance with industry standards within the bio-pharmaceutical sector.
Previous Experience at Janssen Ortho
Mejias Jose held the position of Senior Process Facilitator in the Quicksolvï Business Unit at Janssen Ortho from 1991 to 2004. In this role, he facilitated various processes and managed operations for 13 years, contributing significantly to the company's manufacturing and packaging departments.
Educational Background
Mejias Jose studied at Universidad Del Turabo – Gurabo, P.r and achieved a Bachelor's degree in Natural Science and Chemistry. He completed his studies from 1989 to 1996, gaining a strong foundation in the chemical sciences that he later applied to his extensive career in the pharmaceutical and bio-pharmaceutical industries.
Expertise and Skills
Mejias Jose has over 20 years of experience in the chemical, pharmaceutical, and bio-pharmaceutical industries. He possesses extensive knowledge of GMP’s and FDA regulations for manufacturing processes of medical devices and solution drugs. His skills include excellent planning, organizational, and time management abilities. Mejias demonstrates strong problem-solving, risk analysis, and negotiation skills. He is also adept at managing multiple projects independently and establishing effective working relationships with colleagues, managers, and clients.