Product Quality Engineer

Job content

Job Summary

The Senior Product Quality Engineer will be based at Kallang, Singapore. Mainly responsible to maintain quality engineering programs, standards and improvements within the organization.

What a typical day looks like:

• Participate actively on transferring of new projects from new customer and supporting to set up the NPI product line
• Interface with production , process and test engineering to ensure that products are consistently produced and controlled as per Good Manufacturing Practice (GMP)
• Establish and maintain Quality Control Plan , Risk Management Plan & Report, Device Master Record, FQA Critical component checking plan of the product
• Interface with customers on technical and quality issues and improvement initiatives and provide failure analysis and corrective action reports upon customers’ request
• Responsible for managing customer audits and regulatory and compliance agency audits
• Responsible for authorizing the released of final products to customer and training to FQA personnel and Product Quality Engineering Assistant
• Ensure that the manufactured and shipped products are in compliance with international industrial standards and customer requirements
• Follow up on quality issues identified to ensure corrective actions are in place and effective.
• Work closely with planner, PA, test and process engineers to effectively support for daily manufacturing activities and improve yield
• Participate in internal and external audits of QMS
• Participate in MRB (Material Review Board) review process to make sure timely turnaround of nonconformance material disposition, rework and closure
• Provide factory support to identify and resolve issues associated with purchased parts , materials and manufacturing
• Other relevant duties as assigned

The experience we’re looking to add to the team:

• Diploma/Degree in Mechanical Engineering/Electrical Electronics Engineering/Manufacturing Process Technology
• At least 5 years of manufacturing experience in similar role
• Familiarity in ISO 13485 Quality System Requirements and FDA CFR Part 820 regulations will be an added advantage
• Able to interpret within established procedures and practices as well as exercise independent judgment in complex situations

What you’ll receive for the great work you provide:

• Medical benefits
• Life Insurance
• Paid Time Off
• Allowances and Bonuses*