Ruben C. serves as the Director of Quality Assurance and Regulatory Affairs at Molecular Products, where he leverages over 25 years of extensive experience in quality management systems (QMS) across diverse industries, including medical devices, pharmaceuticals, and automotive manufacturing. In his current role, Ruben is...
Ruben C. serves as the Director of Quality Assurance and Regulatory Affairs at Molecular Products, where he leverages over 25 years of extensive experience in quality management systems (QMS) across diverse industries, including medical devices, pharmaceuticals, and automotive manufacturing. In his current role, Ruben is instrumental in evaluating and refining QMS processes to ensure they are not only efficient but also scalable in alignment with the company’s growth trajectory. His expertise in ISO standards—specifically ISO 9001, ISO 13485, ISO 14001, and ISO 22716—enables him to lead the maintenance and continual improvement of the QMS, ensuring that it meets the rigorous demands of regulatory compliance at all levels of the organization.
Ruben's leadership is pivotal in driving the effectiveness and compliance of Molecular Products with critical regulations such as ITAR and FDA requirements. He spearheads initiatives that foster a culture of continuous improvement, focusing on quality control and process enhancement to optimize operational efficiency. His strategic planning skills are complemented by his ability to train and mentor teams, ensuring that all employees are equipped with the knowledge and tools necessary to uphold the highest quality standards. By integrating advanced methodologies into the manufacturing processes, Ruben not only enhances product quality but also contributes to the overall success and reputation of Molecular Products in the competitive landscape of the medical and pharmaceutical sectors. His commitment to excellence and regulatory compliance positions him as a key asset in driving the company’s mission forward.
