SANTA BARBARA, CA--(Marketwired - December 10, 2013) -
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Wilfredo Santiago will use his background in automated manufacturing equipment commissioning and qualification to help USDM Life Sciences' clients maintain compliance in the manufacturing environment. Santiago brings over 12 years of experience in FDA regulated industries involving medical device, pharmaceutical and biotech product manufacturers. He has provided consulting services to leading brand manufacturers such as Johnson & Johnson, Eli Lilly, Sartorius, Pfizer and Genentech. With his vast knowledge in CSV and strong leadership skills, Santiago will help USDM Life Sciences meet its clients' needs in a quality oriented and timely manner.
"USDM Life Sciences' professional integrity and commitment to fulfill clients' needs are the main reasons I decided to join this remarkable team of experts in the Information Technology, Validation, Risk Management and Regulatory Compliance industries," said Santiago. "I believe that with my experience in manufacturing equipment and automation compliance and Good Automated Manufacturing Practice (GAMP), I can assist USDM Life Sciences in further developing their team in the Manufacturing Systems practice. I look forward to working side by side with the industry's best."
"Wilfredo brings a great deal of experience with automation and equipment validation as well as a proven track record of delivering on projects. We look forward to his leadership and contribution to the Manufacturing Systems practice," said Vega Finucan, Managing Partner of USDM Life Sciences.
About USDM Life Sciences:
USDM Life Sciences is a leading global regulatory consulting firm providing compliance, validation, qualification, quality, auditing and information technology services via project teams and staff augmentation to our clients in the medical device, biotechnology, biologics, diagnostics and pharmaceutical industries. USDM Life Sciences has more than 13 years of experience supplying our clients in the life science industry with compliance services during each phase of their drug and product development cycle while partnering with best of breed organizations to help companies simplify, unify and optimize their business and compliance objectives. For more information, please visit www.usdm.com.
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