PharmaBioServ
Victor Sanchez has extensive work experience in the pharmaceutical industry. Victor began their career in 1996 as a QC Laboratory Supervisor at Schering-Plough Products LLC in Manatí, PR, USA. In this role, they supervised QC laboratories and handled lab investigations, equipment troubleshooting, and method troubleshooting. Victor worked in this position until 2000 when they became the QC Validations Manager at Schering-Plough Products, also in Manatí. As a QC Validations Manager, they were responsible for the recertification of API and finished products during Consent Decree, as well as the validation of analytical methods. In 2004, they joined MSD as the LOCM Operations Manager and later became the LOCM and OSD Operations Manager. In these roles, they managed LOCM and OSD operations. In 2011, they joined Pharma-Bio Serv as the President Europe Operations, where they facilitated FDA readiness and US Regulatory Affairs in Spain. In 2015, they were promoted to the role of President and CEO at Pharma-Bio Serv.
Victor Sanchez has a BS in Chemistry and an MBA in Industrial Management from the Interamerican University of Puerto Rico, which they obtained from 1998 to 2003. Victor later pursued an MS in Pharmaceutical Validation Technology from Technological University Dublin from 2007 to 2010. In 2014, they received a US RAC degree in Regulatory Affairs from the Regulatory Affairs Professional Society. Additionally, they obtained multiple certifications from the Regulatory Affairs Certification Program, including RAPS Membership and RAC-US certification in 2014.
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PharmaBioServ
PharmaBioServ was established in February, 1993, as a service company focused on managing Technology Transfer projects for life science manufacturers. Our original projects expedited new products launch and marketed products optimization and compliance with regulatory agencies requirements. Currently, we are proud to be the largest regulatory compliance and validation company in Puerto Rico, providing its knowledgeable consultants and expertise around the Globe. Having a stable leadership team, the lowest turnover rate in the industry, and five star satisfaction, has allowed us to differentiate ourselves through our consistency, compliance expertise and cost value. Our areas of service include: Project Management, cGMP compliance, Audits, Quality Systems, Remediation, Regulatory Affairs, Qualification and Validation, Contingent Workforce, Personnel Outsourcing, and Training to Pharmaceutical/Biotech, Medical Devices, Food, Cosmetics and related industries. Our diverse team offers an integrated service structure designed to provide complete solutions for our client needs. We also offer educational programs that provide technical courses within a team setting environment. Our main objective is to enhance the understanding of theoretical and practical elements in these industries by providing the latest key skills from well experienced Senior Level resources. Our hands-on workshops, and certifications programs addressing the latest industry trends and regulations. Today, with more than 27 years of experience, we continue to provide our clients with world-class direct contract, consulting, placement and testing services, positioning our company as a global source for efficient and compliant operations.