- Co-founded and led the establishment of four analytical testing laboratories across multiple states, ensuring compliance with ISO 17025 accreditation and complex state regulations. - Spearheaded the company's growth to $18 million in revenue, positioning the Massachusetts location as an industry leader. - Developed and implemented quality management systems to meet regulatory demands and enhance operational efficiency. - Led scientific development, managing a team of 12 across four states, providing mentorship and technical guidance. - Played a key role in partnerships with universities, research institutions, and commercial enterprises to advance the company’s R&D capabilities and ecosystem engagement. - Regularly contributed to state policy evolution concerning safety standards and regulatory frameworks. - Fostered a culture of continuous innovation, positioning MCR Labs as a thought leader in analytical method development and startup support.

MCR Labs is an ISO/IEC-17025:2017 accredited provider of analytical product testing and R&D services committed to assisting manufacturers, patients, researchers, and entrepreneurs. The organization’s team of chemists and pharmaceutical scientists is dedicated to advancing public health and safety through leading-edge chemical analysis of products and offering unparalleled guidance and support for partners, regulators, and community members. For more information visit http://mcrlabs.com.

- Developed and optimized LC/MS/MS methodologies to support pharmaceutical research, with a focus on antibiotic-resistant pathogens. - Led a critical method validation for API impurities, ensuring its seamless integration into production processes. - Collaborated with interdisciplinary teams, providing technical expertise to support drug discovery and preclinical trials. - Presented research findings to senior management and external stakeholders, enhancing the company’s decision-making capabilities.

- Designed and validated preclinical formulations for clients in the biotech and pharmaceutical sectors, specializing in cancer therapies and protein formulations. - Led project management for bioanalytical and formulation development services, successfully navigating GLP regulatory requirements. - Coached and mentored new hires and interns, fostering a high-performance work environment.

Deliver comprehensive material analysis to support internal and external customers in developing new processes and resolving quality issues. Employ SEM techniques to perform visual and elemental characterization of test product and defect materials for the purposes of process enhancement, failure analysis, and quality assurance.

Provided engineering support for a 24/7 printed circuit board manufacturing facility with ownership of eight different wet and dry processes. Developed and maintained processing parameters(SOPs) using SPC tools and methodologies to maximize yield and processing latitude. Evaluated and disposition non-conforming material providing documented rework procedures when necessary. Routinely investigated and resolved scrap and rework events, providing root cause solutions and improving operational performance.