• Global Medical Devices MNC
• Working Location: East

Responsibilities:

• Assure that processes comply with specifications, Quality Systems Regulations and ISO standards.
• Evaluate product/material discrepancies. (PRB/MRB) on time, and implement corrective actions accordant.
• Establish mechanism to evaluate, measure, monitor and/or quality in our products.
• Provide check and balance to manufacturing/system changes submitted by manufacturing Engineers through evaluation/approval of Engineering change request/orders. Ensure update of manufacturing processes in order to reflect quality concepts and specification requirements.
• Support other Quality Engineer improvement and quality activities as needed.
• May provide guidance and assistance to less experienced engineer (eg. Quality Engineer I)
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Ensure that processes comply, with a high confidence level, the tolerances stated on the product specification and drawings.
• Apply statistical tools in order to assure that processes comply with the specifications.
• Conduct failure investigations in order to initiate, stimulate, and assign corrective action.  Issue written reports and update, accordingly.
• Review and analyze quality trends with the manufacturing team. Analyze data based on trends, recommend actions for process, equipment and system improvement.
• Work on product transfers activities and actively participate in product qualifications and validations of equipment and processes.
• Perform risk assessment activities with reliability for product quality risks

Requirements:

• Min Bachelor’s Degree in Engineering qualification is required
• At least 2 years of relevant experience in a quality assurance or test-related capacity related to manufacturing of small electro/mechanical devices,
• Understanding of Statistical Process Controls and use of Minitab software is preferred

To apply, please visit to www.gmprecruit.com and search for Job Reference: 18937

To find out more about this opportunity, please contact Alexandra at: alexandra@gmprecruit.com

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Alexandra Calingo | Registration No: R1101491