PharmEng Technology
Bruce Craven has over 20 years of work experience in the biotechnology and pharmaceutical industry. Bruce started their career as a QA Specialist at Apex Bioscience in 1995 and then worked as a Supervisor at Covance. Bruce then joined Validation Associates Inc. as a Sr. Validation Specialist and later moved to Phoenix Imperative as the Manager of Validation. In 2004, Bruce became the Director of Operations at AMEC BioPharmaceuticals. Bruce then worked as a Sr. Director at BE&K Engineering and later joined KBR (formerly BE&K). In 2009, Bruce became the Vice President and General Manager at Vantage Consulting Group. Bruce then joined Mangan Inc. in 2011 as the President of BioPharm division. Currently, they are employed as the Executive Vice President of PharmEng Technology, where they are responsible for various services related to commissioning and qualification, validation, quality systems, regulatory affairs, engineering, auditing, process development, technology transfer, and training. Bruce has extensive experience in global project management, cleanroom manufacturing support, robotics, automation, controls system engineering, and biocontainment design and engineering.
Bruce Craven obtained a Bachelor of Science (BS) degree in Microbiology from the University of South Carolina, where they studied from 1988 to 1990. Bruce then pursued a Master of Science (MS) degree in Cellular Biology from East Carolina University between 1990 and 1993. Prior to this, Bruce completed a Bachelor of Science (BS) degree in Biology from The Citadel, where they attended from 1986 to 1988.
This person is not in any offices
PharmEng Technology
1 followers
PharmEng Technology is a leading global provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique needs and challenges. At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry. At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).