Jessica De Haan, Pmp
About Jessica De Haan, Pmp
Jessica De Haan, PMP, is a Senior Project Manager, Global Regulatory at Teleflex Incorporated in Morrisville, NC, with over 14 years of experience in project management within the medical device and pharmaceutical industries.
Company
Jessica De Haan is currently employed at Teleflex Incorporated, a global provider of medical technologies. She works in the company's facility located in Morrisville, NC. Her work focuses on managing projects related to global regulatory standards.
Title
Jessica De Haan holds the title of Senior Project Manager, Global Regulatory at Teleflex Incorporated. In this role, she oversees various projects aimed at ensuring compliance with international regulatory requirements. Her leadership is instrumental in maintaining quality and regulatory standards across the company's product lines.
Education and Expertise
Jessica De Haan studied at the Institute of Project Management, where she completed her Project Management Professional (PMP) certification in 2017. She also holds a degree in Marketing/Marketing Management, General from Berkeley College. Her education, combined with over 14 years of experience in project management within the medical device and pharmaceutical industries, has provided her with a robust foundation in regulatory affairs and quality assurance.
Professional Background
Jessica De Haan's professional journey includes several key roles at Teleflex Incorporated. From Labeling Coordinator (2009-2012) to Project Manager (2012-2015), and then Project Manager/Administrative Supervisor, RA/QA Labeling (2015-2016), she has developed extensive expertise in regulatory compliance and project management. Before joining Teleflex, she worked at Sonic Packaging Industries and Reed-Lane, further honing her project management skills.
Experience in Regulatory Affairs and Quality Assurance
In her role at Teleflex Incorporated, Jessica De Haan has led multiple cross-functional teams to ensure adherence to global regulatory standards. Her extensive experience in regulatory affairs and quality assurance, particularly in labeling and documentation, has been crucial in the successful launch of several new medical devices. Her contributions significantly enhance the company's compliance and operational efficiency.