As a Senior Consultant, Angelica brings more than 25 years of engineering experience to MRC Global where she assists clients with quality systems oversight, development and implementation, as well as regulatory affairs, project management, and operations and strategy.
Her depth of experience allows her to provide clients with significant value around quality improvement and regulatory compliance. This includes development of customized quality management systems in compliance with the regulatory requirements applicable to each client’s unique medical device products.
Prior to MRC Global, Angelica was a Senior Regulatory Affairs Manager at Medtronic where she managed international and post-market regulatory teams for the Spine business supporting product lifecycle activities for five manufacturing divisions located throughout the US, Cost Rica, Germany and China. Prior to Medtronic, Angelica was a Regulatory Affairs Manager at Smith & Nephew where she developed strategies to assure regulatory submissions met rigid product launch timelines in identified markets.
Angelica earned her Bachelor of Electrical Engineering, Masters of Manufacture Engineering and an MBA from The University of Texas at El Paso. In addition, she received a Graduate Certificate of Quality of Medical Devices from Christian Brothers University in Memphis, is an ASQ Certified Quality Auditor, 6 Sigma Certified and bi-lingual.