STRATEGIC LEADERSHIP:Develop and implement the company’s vision, mission, and long-term strategies.Drive the overall direction of the company, ensuring alignment with business objectives and market demands.Identify and evaluate growth opportunities, including partnerships, mergers, acquisitions, and new markets.FINANCIAL OVERSIGHT:Manage the company’s financial performance, including P&L, budgeting, forecasting, and financial reporting.Secure funding through venture capital, private equity, grants, or other investment opportunities.Communicate financial performance and growth prospects to investors, stakeholders, and the board of directors.REGULATORY:Ensure that all company activities comply with relevant regulations, including FDA (or other regional authorities) approvals, ISO standards, and other healthcare regulations.Oversee the submission of regulatory documents and liaise with regulatory bodies to ensure timely approval of the surgical devices.Establish and maintain strong ethical standards and practices across the company.LEADERSHIP & TEAM DEVELOPMENT:Build and lead a high-performing executive team and foster a collaborative company culture.Recruit, mentor, and retain top talent in R&D, clinical, regulatory, manufacturing, and commercial roles.Create an inclusive work environment that encourages innovation, accountability, and continuous improvement.STAKEHOLDER MANAGEMENT:Serve as the primary spokesperson for the company, representing it to investors, regulators, healthcare providers, and the media.Develop and maintain strong relationships with key stakeholders, including surgeons, hospitals, academic institutions, and industry partners.Engage with the board of directors to provide updates on company performance and strategic initiatives.Commercialization and Market Strategy:

Product Development:Lead a team of engineering professionals to manage product development cycle and execute concept generation, prototyping all the way to regulatory submission and product commercialization. IP generation and management:Work with IP attorneys to produce and manage patent strategy for the organization.Regulatory Matter:Work with regulatory consultants to strategize products' regulatory pathways and execute regulatory works to ensure our products go through FDA certification.

SingaporeMechanical design of completion/intervention tools including bridge plugs, lubricating valves, annular safety valves, intervention packers, down-hole pressure barrier valves, production packers, down-hole flow control equipment. Completion and Intervention products sustaining includes customization of C&I products mainly on down-hole barrier valve, lubricator valve, fluid saver valve and service tool accessories.Manufacturing support as salvage engineer to inspect, evaluate manufacturing issues.-------------------------United KingdomHalliburton Completion and Intervention (C&I) tools design including down-hole barrier valves, bridge plugs, packers and straddles. Completion and Intervention products sustaining includes customization of C&I products mainly on down-hole barrier valve, lubricator valve, fluid saver valve and service tool accessories.Factory Acceptance Test for aforementioned products and diagnose on issues related to assembly procedure and product design.Development and design of new C&I down-hole tools including retrievable bridge plug, intervention packers and straddles. ISO validation test according for monogram of intervention packers and straddles. Design for testing of pressure vessel for validation at 10000 psi and 325 F.Manufacturing support as salvage engineer to inspect, analyse and dispose work pieces for acceptance or rejection.Engineering skills: Tolerance analysis, mechanism design, stress analysis, DFM, DFA etcEngineering tools used in work include: Solidworks, MathCAD, Excel, PDM etc.