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Peter Shearstone
Vice President, Global Quality and Regulatory at Thermo Fisher Scientific
Professional Background
Peter Shearstone is a notable leader in the field of Global Quality Assurance and Regulatory Affairs, currently serving as the Vice President at Thermo Fisher Scientific. With an extensive background in the life sciences and healthcare sectors, Peter has cultivated a reputation for excellence and innovation throughout his impressive career. His strategic foresight, combined with a strong understanding of regulatory landscapes, has made him a sought-after expert in the complexities of quality assurance and regulatory compliance.
Before joining Thermo Fisher Scientific, Peter held several high-profile roles that contributed significantly to his robust professional background. He served as the Vice President of Regulatory Affairs, Quality Assurance, and Clinical Affairs at Sysmex America, Inc. Here, he led crucial initiatives that enhanced the organization's commitment to delivering safe and effective medical devices. His tenure at Sysmex underscored his ability to bridge the gap between regulatory requirements and practical application, fostering an environment of compliance and quality assurance.
His career also includes a pivotal role as the Lead Director of Regulatory Communications and Program Management at Hospira, a position that saw him at the forefront of navigating complex regulatory frameworks to ensure product safety and efficacy. Peter's expertise in regulatory communications proved invaluable during this period, as he implemented strategies that streamlined processes and improved stakeholder engagement.
At Abbott Diagnostics, Peter served as the Division Vice President of Global Quality Assurance, where he spearheaded initiatives that assured product quality and compliance across various global markets. This experience further solidified his reputation as a leader in quality assurance, enabling him to bring valuable insights into the dynamics of global healthcare.
In addition, Peter's prior role as the Vice President of Global Quality Assurance at Siemens Healthcare showcased his capacity to manage large-scale quality operations and regulatory affairs while maintaining a steadfast commitment to quality and safety. His early career also included a managerial position in Quality at Tenax, where he laid the groundwork for his later achievements in quality management and regulatory affairs.
Education and Achievements
Peter Shearstone's educational journey began at Bridgewater Raynham Regional High School, where he focused on a College/University Preparatory and Advanced High School/Secondary Diploma Program. This foundation equipped him with the critical thinking and analytical skills necessary for success in higher education and beyond.
He advanced his studies at Salem State University, earning a Bachelor of Science (BS) in Biology, General. This scientific background has played a pivotal role in shaping his understanding of the biological aspects necessary for working in the healthcare and life sciences industries. His education has also underscored the importance of scientific rigor and ethical standards in regulatory affairs and quality assurance, making him an effective advocate for improving health outcomes through safe medical devices and diagnostics.
Peter's achievements in the industry are marked by his ability to navigate challenging regulatory environments and his commitment to continuous improvement in quality management practices. His leadership in various organizations has not only enhanced their regulatory compliance but also significantly contributed to innovation and excellence in the healthcare sector.
Achievements
- Vice President, Global Quality Assurance and Regulatory Affairs at Thermo Fisher Scientific: Leading strategic initiatives aimed at enhancing quality and compliance standards across the organization, impacting healthcare globally.
- Former VP at Sysmex America, Inc.: Drove significant improvements in regulatory affairs and clinical quality, ensuring the utmost safety and efficacy of medical devices.
- Lead Director at Hospira: Managed regulatory communications and ensured the company effectively navigated complex regulatory frameworks, enhancing stakeholder relationships.
- DVP at Abbott Diagnostics: Oversaw global quality assurance initiatives, reinforcing Abbott’s commitment to product quality and regulatory compliance.
- VP at Siemens Healthcare: Managed global quality assurance efforts, impacting the company’s operational excellence and commitment to patient safety.
- Early Career at Tenax: Developed foundational skills in quality management, setting the stage for later accomplishments in regulatory affairs and quality assurance.