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Derrick Loud
Associate Manager, Post Market Quality at BD
Professional Background
Derrick Loud is an accomplished Biomedical Engineer with a strong focus on Post Market Quality and an impressive track record in the medical device industry. With his analytical mindset and extensive knowledge, he has established himself as a leader in his field. Currently, he serves as the Associate Manager of Post Market Quality at BD, where he applies his expertise to ensure the highest quality standards in medical devices. His responsibilities include conducting thorough complaint investigations, performing post-market trending analysis, overseeing Corrective and Preventive Actions (CAPA), and managing field actions, all aimed at maintaining product safety and efficacy.
Before his role at BD, Derrick held various positions at CR Bard, where he progressed from Field Assurance Engineer to Field Assurance Engineer II. In these roles, he was responsible for managing risk assessments in compliance with ISO 14971 and fostering adherence to Quality Management Systems as per ISO 13485. His effective communication skills and attention to detail facilitated his preparedness for FDA and Notified Body audits, further solidifying the company’s regulatory compliance and operational integrity.
Furthermore, Derrick's entrepreneurial spirit is showcased in his experience as the Designer and Founder of BOOGÜD, demonstrating his innovative mindset and capability to navigate the complexities of the biomedical landscape. Earlier in his career, he gained invaluable experience as a Lab Technician at GenLife Institute, where he honed his foundational skills in bioengineering, setting the stage for his future successes.
Education and Achievements
Derrick Loud pursued his higher education at Arizona State University, earning both a Bachelor of Science (BS) and a Master of Science (MS) in Bioengineering and Biomedical Engineering. His solid educational background has equipped him with a comprehensive understanding of the intricate design, development, and regulation of medical devices.
His educational journey instilled in him not only technical knowledge but also critical thinking and problem-solving skills, essential for navigating the rapidly evolving medical technology landscape. His graduate studies focused on advanced topics in bioengineering, allowing him to deepen his skills in quality assurance and risk management, making him a sought-after professional in the industry.
Achievements
Throughout his career, Derrick has accumulated numerous achievements that highlight his exceptional capabilities and contributions to the biomedical engineering field. His expertise in Post Market Quality has significantly impacted product quality and patient safety in the organizations he has worked for. At BD, he has successfully led multiple projects that resulted in improved processes for complaint handling and CAPA implementations.
Derrick's role in preparing for FDA and Notified Body audits has shown his commitment to regulatory compliance and his ability to anticipate challenges, ensuring smooth audit processes and fostering trust with stakeholders. His analytical approach to risk management per ISO 14971 has also made him a key player in advancing industry standards within the field of biomedical engineering.
Combining his technical skills with a passion for quality and safety, Derrick Loud continues to excel as a leader in the biomedical engineering sector, driving innovation and improvement in medical device quality and regulation.