Enable job alerts via email!
Boost your interview chances
Create a job specific, tailored resume for higher success rate.
Ein innovatives Unternehmen sucht einen Engineering Assistant für Qualitätsmanagement, um sicherzustellen, dass alle Produkte den Qualitätsanforderungen entsprechen. In dieser spannenden Rolle sind Sie für die Verwaltung von Kundenbeschwerden, die Unterstützung bei der Qualitätsprüfung und die Schulung von Mitarbeitern verantwortlich. Sie werden Teil eines dynamischen Teams, das sich der Verbesserung der Produktqualität und der Einhaltung von Standards widmet. Wenn Sie eine Leidenschaft für Qualität und Innovation haben, ist dies die perfekte Gelegenheit für Sie, in einem globalen Unternehmen zu wachsen und einen echten Unterschied zu machen.
Venture, a public listed company in SGX, is a leading global provider of technology services, products and solutions with established capabilities spanning marketing research, design, research and development. Over the years, Venture has built know-how and intellectual property with expertise in several technology domains. These include life science & genomics, molecular diagnostics, medical devices and equipment, healthcare and wellness technology, lifestyle consumer technology, health improvement products, instrumentation, test and measurement technology, networking and communications, fintech, as well as computing, printing and imaging technology.
Headquartered in Singapore, the Group comprises over 30 companies with global clusters in Southeast Asia, Northeast Asia, America and Europe, and employs over 12,000 people globally.
At Venture, our people are our most valuable asset. We are committed to unifying culture, encouraging innovation, and harnessing the collective strengths and synergies of our human capital to deliver compelling differentiation, advancing Venture’s position as a leading global provider of technology solutions, products and services.
We’re looking to add a Engineering Assistant, Qualityin Singapore. The position is based in our GES site at Marsiling.
As a Engineering Assistant, Quality, you will:
Be responsible for ensuring all product quality, process quality and system conform to customers’ specifications and internal quality system requirements.
JOB RESPONSIBILITIES
Managing all customer complaints, feedbacks, and returns till complete closure
Monitoring and improving customer complaints and customer returns rate
Attending to all customer periodic audits, review meetings and visits
Managing a team of inspectors in achieving the targets set by the management
Supporting NPI activities for ODM and OEM products
Draft, maintain and update of Quality Work Instruction / Manufacturing Instructions and In-Process Quality Checklist
Monitoring and improving the products quality performance to meet or exceed the quality targets set by the management or customer
Participate in weekly NCMR meeting to drive down inventory in MRB location
Verification of Customer Return Unit before accepting to in-stock
Raise Quality Alert for all non-conformance/workmanship and customer feedback
Prepare, Raise and close Purge Order Activities
Preparing weekly and monthly quality reports
Participating in weekly MRR meeting to drive down inventory at MRB location
Conducting quarterly ESD audit
Conducting products quality training to all inspectors and technicians
For Medical Products:
Ensure all Device History Records are effectively and accurately recorded as per Good Documentation Practice and Quality System requirements
Ensure that Device History Records are scanned and uploaded to Database on a timely manner.
Retrieve Device History Records as per request by customer.
Authority:
Improving all quality- related documents, eg. Manufacturing instructions, inspection checklists, inspection plans, etc
Providing disposition for nonconforming materials/ products.
Determining the acceptance level of the products quality.
Purging and recalling nonconforming materials and finished goods.
Stopping production processes and deliveries and in the event of any product nonconformance being detected during QA/ Customer inspections/ tests
Sign off SRV form and QA Inspection Checklist
Sign off NCMR for disposition
EDUCATION and EXPERIENCE
Diploma holder with at least 2 years of Quality Management experience
Experienced applicants must have at least 2 years of hands-on experience in Quality Assurance activities
Experience in Medical Devices manufacturing processes is preferred.
Basic knowledge on Microsoft office, PPAP, FMEA, Control Plan, Quality Plan, QC Seven Tools, CAPA Methodology (ie. Using 8D, 5-whys, Fish-bone etc) and StatisticalTechniques.
Able to interpret basic technical drawing, component datasheet, schematic diagram, inspection checklist and sampling plan table.
Able to use basic QC measuring equipment.
Basic knowledge of ISO 9001, ISO13485, ISO14001, FDA 21 CFR Part 820 & Part 11 Quality System Requirements. Knowledge of the basic elements of Good Manufacturing Practices (GMP) in a manufacturing environment and the ability to apply them.
If you embody the spirit of excellence, passion for discovery, innovation and enterprise, and the desire to make a difference in the world of technology and electronics, come join the Venture team!
Be Part of the Venture Family.