Kranthi Dhamuluri

As the Founder and CEO of Intellectt Inc., I spearheaded the establishment and growth of the company, overseeing all aspects of business operations, including strategy, sales, and service delivery. I drove significant growth by developing innovative solutions, streamlining processes, and fostering a culture of excellence. My leadership focused on digital transformation, engineering expertise, and building a successful, diverse global team.

• Developed strong partnerships with other businesses to allow for collaboration and more significant opportunities for growth.
• Established a successful business by identifying market needs and developing innovative solutions.
• Delivered exceptional customer service by addressing client concerns promptly and effectively resolving issues.
• Led the strategic planning process to define business goals and ensure alignment across all departments.
• Built a positive organizational culture that fostered creativity, innovation, and employee engagement.

I led technical teams in the development and implementation of healthcare solutions, ensuring alignment with project goals and regulatory standards. I managed project timelines, facilitated cross-functional collaboration, and drove innovation to optimize operational efficiency and deliver high-quality outcomes.

• Coordinated with other departments effectively, integrating technical requirements into broader organizational goals seamlessly.
• Managed implementation of new technological improvements resulting in increased efficiency.
• Built trusted relationships with stakeholders through clear communication and collaborative problem-solving efforts.
• Guided, coached and lead project teams, delegating tasks and evaluating performance and progression of project pace.
• Met with clients to gather and understand requirements and coordinated with system administrators and directors to plan and schedule project activities.
• Recruited and trained IT team members.
• Evaluated reputation risk and regulatory risk.

As a Product Engineer at Medtronic, I was responsible for designing, developing, and testing medical devices to meet regulatory standards and customer needs. I collaborated with cross-functional teams to improve product performance, conducted failure analysis, and implemented design modifications to enhance product reliability and efficacy.

• Provided clear and timely technical data required for design and specification of product.
• Provided technical support to sales teams, enabling them to better communicate product benefits and features to customers.
• Streamlined the production process for increased efficiency and reduced manufacturing times.
• Optimized supply chain management, reducing material costs while maintaining high-quality standards.
• Launched customer-driven design review process to enhance customer experiences and efficiency.

As a Quality Analyst at Novel Laboratories, Inc., I was responsible for conducting quality control tests and inspections to ensure compliance with industry standards and regulatory requirements. I analyzed and documented test results, identified defects, and implemented corrective actions to maintain high product quality and consistency.

• Analyzed quality and performance data to support operational decision-making.
• Created and revised procedures, checklists and job aids to reduce errors.
• Developed training materials, SOPs and work instructions to supplement new team member onboarding.
• Collaborated with cross-functional teams to develop and implement targeted solutions for identified quality issues, ensuring continuous improvement.
• Recorded findings of inspection process, collaborating with quality team to implement corrective actions.

As a Regulatory Affairs Associate at Freyr Solutions, I ensured compliance with regulatory requirements and assisted in the preparation and submission of regulatory documents. I supported regulatory strategy and maintained up-to-date knowledge of relevant regulations and guidelines.

• Consolidated global information relevant to [Product or Service] and monitored global submissions and approvals status.
• Conducted thorough reviews of labeling content for accuracy and adherence to relevant regulations before submission to authorities.
• Performed and documented quality control checks to maintain compliance with company initiatives.