I am a professional with over 15 years of experience in the biopharmaceutical and public health industry. My extensive experience within Quality assurance, regulatory, biopharmaceutical manufacturing, and public health has provided me with exceptional perspective that has allowed me to be recognized as a top performer in quality control, quality management systems and project management throughout my career. I have worked in both management and as an individual contributor in the pharmaceutical industry that demonstrates my abilities as a result oriented, driven individual that is able to work well with all levels within an organization. I am a strategic leader and build consensus to empower my team. I have extensive knowledge and experience with quality systems and processes, current good manufacturing practices (cGMP), regulatory compliance and good laboratory practices (GLP), and various international public health regulations. I also have experience in delivering complex multi-disciplinary projects within a highly regulated environment, develop and deliver technical and high level presentation to senior leadership, which has helped me become proficient in identifying and organizing continuous improvement projects and initiatives that ensure compliant, sustainable, and costeffective processes. As an ambitious, determined, and qualified individual, I have acquired expertise in many areas of the pharmaceutical and public health industry including Program management, Compliance management, Quality Control, Supply Chain, Quality Assurance and Manufacturing. Additionally, I have managed and led global technology/SaaS programs worth over $100million. I worked with and was the liaison of the global project team and client project team, vendors, certification bodies, to accomplish and deliver project/program goals.
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