Pablo Batista
About Pablo Batista
Pablo Batista is a Senior Process Engineer with extensive experience in the pharmaceutical and biotech industries, currently working at Teva Pharmaceuticals, Amgen, and Bristol-Myers Squibb.
Title and Current Roles
Pablo Batista holds the title of Senior Process Engineer. He is currently working at several prominent pharmaceutical companies including Teva Pharmaceuticals as a Validation Engineer in Florida, Amgen as a Scientist, and Bristol-Myers Squibb as a Senior Process Engineer in Manati, PR.
Previous Positions in the Pharmaceutical Industry
Pablo Batista has held various roles in the pharmaceutical industry. From 2011 to 2014, he worked at Janssen as a Pharmaceutical Scientist (Technical Services) in Gurabo and at Warner Chilcott as a Pharmaceutical Scientist (Contractor) in Fajardo, PR. He also has experience from working in engineering and consultancy roles that have spanned multiple companies and functions over his career.
Engineering and Consulting Experience
From 2006 to 2011, Pablo Batista's career included roles at Stantec as a Process Engineer and at Perry Products Div. of Servimetal as a Consulting Engineer in Guaynabo and Caguas, PR, respectively. He was also an Inside Sales Engineer at Engineering Parts & Services in Dorado, PR from 2004 to 2006, and a Field Engineer at S&D Engineering in Toa Baja, PR from 2003 to 2004. Earlier in his career, he worked as a QA/QC Engineer at Barrett, Hale & Alamo in San Juan, PR from 1999 to 2002.
Educational Background in Mechanical Engineering
Pablo Batista studied Mechanical Engineering at the Universidad Politécnica de Puerto Rico, where he obtained his Bachelor's degree after studying from 1996 to 2003. This strong educational foundation has supported his extensive career in process engineering.
Skills and Expertise in the Pharmaceutical Industry
With over 10 years of experience, Pablo Batista is skilled in process development, process validations, and process execution. He has significant expertise in structuring processes within regulated environments, emphasizing quality and business orientation. His proficiency in quality risk management, Lean Manufacturing, and Six Sigma concepts is notable, along with his experience in project management and leading multidisciplinary teams. He is familiar with multiple pharmaceutical technologies including sterile, parenteral/injectable, solids, semi-solids, liquids, and devices.