Maintains quality engineering programs, standards and improvements within the organization.
Develops and initiates standards and methods for inspection, testing and evaluation based on medical device standards
Devise sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data.
Develops and implements methods and procedures for disposition of discrepant materials.
Directs inspection team engaged in measuring, inspecting and/or testing products or parts and tabulating data concerning materials, product or process quality and reliability.
Executes the inspection / testing of new equipment capability
Supervises inspection team on the inspection plan
Supports Product Engineering and Program Manager with customer interfaces as necessary on quality related issues.
Provides liaison to various regulatory bodies
Responsible for authorizing the released of final products to customer
Contributes to the workplace safety and health improvement for the employees, as well as environmental protection, by adhering to the company's Environmental, Health and Safety policies and procedures, and helping to achieve EHS objectives and targets through participation of EHS programs
Participate and adhere to Corporate Social and Environmental Responsibility (CSER) policy, programs and procedures.
Requirements:
Singaporeans ONLY
Diploma / Degree in Mechanical Engineering / Electromechanical Engineering / Electronics Engineering/Manufacturing Process Technology or related discipline, preferably with at least 3-5 years relevant experience in manufacturing environment.
Familiar with ISO 13485 Quality System Requirements / US Food and Drug Administration (FDA) / CFR Part 820 regulations.
Familiarity with inspection equipment, statistical tools, Geometric Dimension and Tolerance knowledge will be an advantage.