Pearl Pathways Hires Phillip Bishop
INDIANAPOLIS, INDIANA – November 17, 2016 — Pearl Pathways announces the hiring of Phillip Bishop as a Quality Analyst serving medical device and biopharmaceutical life science companies.
Bishop brings 13 years of quality control (QC) laboratory experience to the Pearl Pathways team and recently held leadership roles in a good manufacturing practice (GMP) compliant QC laboratory at a top-tier contract manufacturer of sterile products. In previous roles, Bishop led a team of analysts to ensure that the release and QC tests were performed for both in-process and completed manufactured products. Bishop’s in-depth knowledge of multiple test methods, typical compendial procedures, endotoxin testing, and his advanced understanding of quality system processes and global health regulatory body requirements make him a valuable addition to the team. Bishop holds a Bachelor of Science in Biology from the University of Indianapolis.
Diana Caldwell, President and CEO shares, “Phillip brings strong quality, manufacturing, and technical expertise as well as a deep understanding of validation documentation to the Pearl team. Our clients will benefit from his vast knowledge of quality compliance and quality assurance systems, CAPA, multiple test methods, and pharmacopeial work. He has broad work experience having also worked as a subject matter expert for an endotoxin testing facility. We are thrilled to have Phillip join the team.”
About Pearl Pathways
Pearl Pathways is a comprehensive life science product development services company. Our experienced team is obsessed with expediting life science product development regulatory pathways. We have three business units to serve you:
Pearl IRB is a full service commercial Independent Review Board that provides human research IRB reviews, IRB exemptions and waivers, and also offers support for research protocol/ICF medical writing, site assessments, and monitoring services.
Pearl ReGXP is a regulatory and quality compliance consulting practice that provides regulatory filing guidance, conducts global health authority negotiations, develops/improves quality systems, and delivers GMP/GLP/GCP auditing services.
Pearl IDEAS provides strategic product development assistance, third party vendor selection and management strategies, due diligence services, and sales and marketing services for drug, biologic and device companies.
To learn more, please visit us at www.pearlpathways.com, call us at (317) 899-9341, or email firstname.lastname@example.org. Pearl Pathwaysis located in Indianapolis, Indiana, and isAAHRPP accredited and a WBENC certified woman owned business. For media inquiries, contact email@example.com.